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Design of a prospective, multicenter, global, cohort study of electromagnetic navigation bronchoscopy



Electromagnetic navigation bronchoscopy (ENB) procedures allow physicians to access peripheral lung lesions beyond the reach of conventional bronchoscopy. However, published research is primarily limited to small, single-center studies using previous-generation ENB software. The impact of user experience, patient factors, and lesion/procedural characteristics remains largely unexplored in a large, multicenter study.


NAVIGATE (Clinical Evaluation of superDimension™ Navigation System for Electromagnetic Navigation Bronchoscopy) is a prospective, multicenter, global, cohort study. The study aims to enroll up to 2,500 consecutive subjects presenting for evaluation of lung lesions utilizing the ENB procedure at up to 75 clinical sites in the United States, Europe, and Asia. Subjects will be assessed at baseline, at the time of procedure, and at 1, 12, and 24 months post-procedure. The pre-test probability of malignancy will be determined for peripheral lung nodules. Endpoints include procedure-related adverse events, including pneumothorax, bronchopulmonary hemorrhage, and respiratory failure, as well as quality of life, and subject satisfaction. Diagnostic yield and accuracy, repeat biopsy rate, tissue adequacy for genetic testing, and stage at diagnosis will be reported for biopsy procedures. Complementary technologies, such as fluoroscopy and endobronchial ultrasound, will be explored. Success rates of fiducial marker placement, dye marking, and lymph node biopsies will be captured when applicable. Subgroup analyses based on geography, demographics, investigator experience, and lesion and procedure characteristics are planned.


Study enrollment began in April 2015. As of February 19, 2016, 500 subjects had been enrolled at 23 clinical sites with enrollment ongoing. NAVIGATE will be the largest prospective, multicenter clinical study on ENB procedures to date and will provide real-world experience data on the utility of the ENB procedure in a broad range of clinical scenarios.

Trial registration NCT02410837. Registered 31 March 2015.

Peer Review reports


Lung cancer is the leading cause of cancer death among both men and women in developed countries globally. An estimated 1.8 million new cases of lung and airway cancers occurred worldwide in 2012 [1].

Rapid and precise diagnosis of suspicious lesions is crucial to determine the optimal treatment for abnormalities in the lung found on chest computed tomography (CT) imaging. According to the American Cancer Society’s 2015 estimates, the 5-year survival rate for distant (metastasized) lung cancer is 4 %, compared to 27 % for regional cancer and 54 % for localized cancer. However, few lung cancers are diagnosed at an early stage when more patients are amenable to curative treatment options [2].

The National Lung Screening Trial [3] clearly demonstrated the efficacy of screening in a defined high-risk subset of the population. While the results and their generalizability can be questioned, the trial established the utility of low-dose CT scanning over conventional chest radiography. In addition, declining costs of technology, greater availability of CT imaging, lower radiation dosing, and increased awareness all have led to more CT scans of the chest. These scans will inevitably identify abnormalities for which intervention may be necessary. Current diagnostic options include image-guided needle biopsy, surgery, and more recently, electromagnetic navigation bronchoscopy.

ENB is an image-guided approach that uses 3D-reconstructed CT-scan and sensor location technology to guide a steerable endoscopic probe to peripheral lung lesions that may be beyond the reach of conventional bronchoscopes [4, 5], potentially aiding in diagnosis of lung cancer at an early stage of disease. This technology will also allow diagnosis of pulmonary metastases or benign diseases, such as infectious lung lesions or granulomatous disease, without surgical incisions.

Table 1 summarizes 24 original research articles published to date on the use of ENB procedures to aid in the diagnosis of peripheral lung lesions [629], most of which have been summarized in several meta-analyses [3032]. In the most recent meta-analysis, the pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio were 82 %, 100 %, 19.36, 0.23, and 97.62, respectively [32]. The pooled pneumothorax rate was approximately 3 %, of which approximately 1.6 % required chest tube insertion [30].

Table 1 Prior clinical studies on ENB to aid in the diagnosis of peripheral lung lesions

ENB procedures can also be used to aid in the diagnosis of mediastinal lymphadenopathy [33], as a localization tool for dye marking prior to video- or robotic-assisted thoracoscopic surgery [34], or to place fiducial markers prior to stereotactic body radiation therapy [35], all in a single procedure.

Despite these promising results, outcomes following ENB procedures are widely varied and most evidence to date is based on single-center analyses. Of the 24 published original studies on the use of ENB procedures to aid in the diagnosis of peripheral lung lesions, only 4 studies were multicenter [9, 10, 19, 29] and only 5 enrolled greater than 100 subjects [12, 20, 21, 28, 29] (see Table 1). The impact of user experience, patient risk factors, and lesion/procedural characteristics remains largely unexplored in a large multi-center study. The lack of clearly defined performance outcomes, varied definitions of diagnostic yield and accuracy, inconsistent use of complementary techniques, such as radial endobronchial ultrasound (EBUS), use of older ENB software versions, and variability in lesions targeted and biopsy methods also challenge the interpretation of results across studies. In addition, the full profile of how ENB procedures are used in daily practice (e.g., peripheral versus central lesions, lymph node sampling, dye marking, and fiducial marker placement) is not well understood. As ENB usage increases and is adopted by community centers with a wide range of user experience levels, the full safety profile across diverse clinical scenarios must be well understood, particularly with respect to the patient, lesion, and procedural factors associated with performance outcomes.

NAVIGATE (Clinical Evaluation of superDimension™ Navigation System for Electromagnetic Navigation Bronchoscopy) aims to enroll up to 2,500 consecutive subjects at up to 75 sites worldwide. When complete, NAVIGATE will be the largest prospective, multicenter clinical study of ENB procedures to date. The objective of this observational study is to evaluate the safety profile and outcomes following ENB procedures conducted for suspicion of cancer or other diseases in lung lesions, for lymph node biopsy, or for dye marking or fiducial marker placement. The study is designed to capture the real-world experience of ENB use across heterogeneous sites and geographies, without restriction on ancillary tools or procedures. The 24-month follow-up will also allow an assessment of long-term diagnostic accuracy and the correlation between stage of diagnosis and short-term survival rates.


Ethical compliance

This study is being conducted in accordance with the Declaration of Helsinki and all local regulatory requirements. As of February 19, 2016, 23 clinical sites in the United States and Europe had been activated into study (see Additional file 1 for the list of activated sites to date). The protocol was approved by the institutional review board of each participating site. Additional site selection is ongoing. Institutional review board approval will be obtained for each newly activated site prior to subject enrollment. Inclusion of up to 75 clinical sites is prespecified per protocol. The study was registered under identifier NCT02410837 on March 31, 2015, which will be updated as new sites are activated. All subjects have provided or will provide written informed consent prior to enrollment.

Trial design and subject eligibility

NAVIGATE is a prospective, single-arm, multicenter, post-market, observational study of ENB procedure use. The study aims to enroll up to 2,500 subjects at up to 75 clinical sites worldwide, including the United States, Europe, China, Korea, and Japan. To ensure heterogeneity of the data, a maximum enrollment per site will be specified for each region, approximately 75 subjects per site in the US, with other regions to be determined.

All consecutive patients over the age of 18, who are candidates for an elective ENB procedure and who present for evaluation of lung lesions, are eligible for enrollment. Exclusion criteria are: (1) the patient is unable or unwilling to provide informed consent or to comply with study follow-up schedule; (2) the patient has participated in an investigational drug or device research study within 30 days of enrollment that would interfere with this study; and (3) the patient is pregnant or nursing.

Test device

The superDimension™ navigation system, software version 6.0 or higher (Medtronic, Minneapolis, MN), will be used to conduct all ENB procedures [46, 8].

Pre-procedure assessments

A full list of subject demographics, lesion characteristics, and pre-procedure data to be collected is included in Table 2.

Table 2 Study assessments

In addition, to assess the value of the ENB procedure as a decision-making tool, the pre-procedure probability of malignancy will be assessed for each subject being evaluated for diagnosis of a pulmonary nodule [36, 37]. Probability will be captured both by the investigator’s subjective estimation of pretest probability of malignancy and a mathematical model, to allow comparison between the two methods. The probability model employs a multiple regression equation including the following factors: (1) subject age; (2) smoking history; (3) history of extrathoracic malignancy; (4) nodule size; (5) nodule border characteristics; and (6) nodule location (see Additional file 2 for the full equation). See Additional file 3 for the definition of peripheral lung lesions.


The ENB procedure will be performed per product instructions and the institution’s standard practice. All complementary devices and procedures (e.g., catheter type, biopsy tools, access tools, fiducial placement or dye marking, and concomitant imaging, such as radial EBUS) are at the discretion of the investigator and are not mandated per the study protocol. All complementary procedures and devices will be captured (Table 2).

Primary and secondary endpoints

This post-market study is intended to capture clinical outcomes related to the real-world use of ENB procedures, including but not limited to peripheral lesion biopsies, lymph node biopsies, fiducial marker placement for radiation therapy, and tumor marking for diagnostic and therapeutic surgery.

The primary endpoint is the incidence of pneumothorax related to the ENB index procedure rated as Grade 2 or higher according to the Common Terminology Criteria for Adverse Events (CTCAE) scale (Table 3) [38]. The primary endpoint was chosen as a comprehensive endpoint that would be applicable to all ENB procedures. The secondary endpoints will be assessed as applicable to the ENB procedure being conducted.

Table 3 Study definitions

The following secondary endpoints will evaluated for all ENB index procedures:

  1. 1.

    Incidence of all pneumothoraces related to ENB index procedure

  2. 2.

    Incidence of bronchopulmonary hemorrhage related to ENB index procedure rated as Grade 2 or higher according to the CTCAE scale

  3. 3.

    Incidence of respiratory failure related to ENB index procedure rated as Grade 4 or higher according to the CTCAE scale

  4. 4.

    Subject health status and quality of life evaluated by EQ-5D-3 L questionnaire (Version 5.1, April 2015) [39, 40]

  5. 5.

    Subject self-reported satisfaction at 1-month post-procedure, including referral source, pre-procedure expectations, pain, willingness to undergo another ENB procedure, worker productivity, and willingness to recommend the ENB procedure to family and friends.

  6. 6.

    ENB procedure effect on subject productivity and activity using the ENB Productivity and Activity Questionnaire (ENB-PAQ) at 1-month visit.

The following secondary endpoints will be evaluated for all ENB index procedures performed for suspicion of cancer or other diseases in a lung lesion. See Table 3 for definitions.

  1. 7.

    Diagnostic yield

  2. 8.


  3. 9.


  4. 10.

    Positive predictive value

  5. 11.

    Negative predictive value

  6. 12.

    Repeat biopsy rate due to lack of diagnosis during ENB index procedure

  7. 13.

    Adequacy of sample for molecular testing and mutation type (if applicable)

  8. 14.


  9. 15.

    Stage at diagnosis (if applicable)

In addition, the following secondary endpoints will be evaluated for applicable procedures:

  1. 7.

    Success rate of accurate placement of fiducial markers demonstrated through follow-up imaging

  2. 8.

    Success rate of dye marking demonstrated by successful surgical resection

  3. 9.

    Success rate of obtaining lymph node biopsy to provide stage of diagnosis

In addition to the primary and secondary endpoints listed above, all adverse events related to the ENB procedure or associated tools will be captured and reported, including all incidences of death, pneumothorax, bronchopulmonary hemorrhage, and respiratory failure regardless of CTCAE grade. New scales have also been developed by the study investigators and validated by expert consensus (Delphi technique [41]) to provide more specific criteria for defining the incidence and severity of bronchopulmonary hemorrhage and pneumothorax in subjects undergoing transbronchial lung biopsies under flexible bronchoscopy. These scales will be evaluated for the first time in the NAVIGATE study and compared to the existing CTCAE scale (E. Folch and S. Khandhar, unpublished personal communication; publication in progress). Additional procedural and follow-up assessments are listed in Table 2.


Subjects will be evaluated at baseline (within 30 days of the procedure), on the procedure day, and at 1 month, 12 months, and 24 months post-procedure. Follow-up will capture any repeat diagnostic procedures or new diagnoses on any lung nodule evaluated during the initial ENB index procedure, as well as healthcare utilization since the ENB index procedure (including healthcare visits, repeat ENB procedures, transthoracic biopsy, bronchoscopy, chemotherapy, brachytherapy, radiation therapy, surgical resection, and lymph node dissection). All lung nodules evaluated during the initial ENB index procedure will be followed for confirmation of ENB-aided diagnoses, including confirmation of initially negative or inconclusive results.

Investigator training

All investigators must have completed the superDimension™ navigation system training course prior to enrolling subjects into the study. In order to capture the full breadth of ENB procedure usage at both high-volume and low-volume centers, investigators without extensive experience conducting ENB procedures will be allowed to perform a maximum of 5 “roll-in cases”.

Roll-in subjects will be considered study participants and will complete all protocol-required procedures and follow-up. However, data for the roll-in group will be analyzed separately from the remaining study population in an effort to detect any differences in outcomes related to the level of investigator experience.


No sample size calculations were conducted for this single-arm, observational study. All statistical analyses will be performed using Statistical Analysis System (SAS) for Windows (Version 9.2 or higher, SAS Institute Inc. Cary, NC) or other widely accepted statistical or graphical software.

Descriptive statistics will be used to present the data and to summarize the results. Discrete variables will be presented using frequency distributions and cross tabulations. Continuous variables will be summarized by presenting the number of observations (n), mean, standard deviation, median, minimum, and maximum values. For the primary endpoint, a 2-sided 95 % exact binomial confidence interval will also be provided.

In general, data analysis will be conducted on all subjects who are enrolled in the trial and undergo an ENB procedure. Analyses will be conducted on multiple subsets of study subjects based upon variables such as geography, demographics, investigator experience, lesion and procedure characteristics, and other variables as deemed appropriate. Multifactorial and subgroup analyses evaluating the impact of patient (e.g., medical and surgical history, risk profile), lesion (e.g., size, location), and procedural characteristics (e.g., rapid on-site evaluation use, tissue adequacy, anesthesia method, use of complementary technology) are planned.

Interim analyses are prespecified per protocol when the first 500, 1000, and 1500 subjects enrolled reach the 1-month and 1-year follow-up timepoints.

Study organization

The sponsor will utilize a medical monitor to provide a medical review and adjudication of pre-specified adverse events in support of the protocol-defined endpoint data. The medical monitor is a qualified, board-certified physician who is not affiliated with an investigative center or the study sponsor.

In addition, a global Investigator Steering Committee will provide oversight of study conduct, data analysis, subject safety, and the publication of results in alignment with recommendations of the International Committee of Medical Journal Editors.

Enrollment status

Enrollment began in April 2015 and is currently in progress. As of February 19, 2016, 500 subjects had been enrolled at 23 clinical sites in the United States and Europe. An interim analysis of the 1-month follow-up of this first cohort is planned for the fall of 2016, with a focus on patient and lesion characteristics and usage profile. Study enrollment is progressing on schedule to reach the planned number of approximately 2,500 subjects; however, final enrollment numbers are not guaranteed.


Current guidelines for the evaluation of patients suspected of having lung cancer recommend the least invasive method appropriate to the patient’s medical presentation, with flexible bronchoscopy as the first line approach for central lesions [42]. For peripheral lesions difficult to reach with conventional bronchoscopy, options include percutaneous transthoracic CT- or fluoroscopy-guided techniques or guided bronchoscopy. While transthoracic needle aspiration (TTNA) is preferred due to its high diagnostic yield, in a meta-analysis of 20 studies the mean pneumothorax rate was 25 % (range 4.2 %–60 %) [43].

Guided bronchoscopic methods include ENB, radial EBUS, and virtual bronchoscopy. A meta-analysis of guided bronchoscopic methods found that the weighted diagnostic yield of these techniques was higher than that of traditional bronchoscopy but lower than the typical yield of TTNA, with a wide variation among studies [31]. Radial EBUS has a low pneumothorax rate (approximately 1 %), similar to that of ENB. Like ENB, studies of radial EBUS-guided localization have reported varied outcomes dependent on user experience, with sensitivity for detection of malignancy ranging from 49 % to 88 % and a pooled sensitivity of 73 % [44]. Radial EBUS can be used in conjunction with ENB to confirm tumor location after initial navigation with ENB, with higher diagnostic yield than either procedure alone [9]. However, radial EBUS has been shown to have a lower diagnostic yield in lesions ≤20 mm in size [44]. Virtual bronchoscopy using an ultrathin bronchoscope, may also improve diagnostic yield when combined with radial EBUS, but is not widely available and is limited by the lack of a working channel for biopsy [45].

ENB procedures provide a minimally invasive, alternative method to access peripheral lung lesions and offer the potential for biopsy, fiducial marker placement, and/or dye marking in a single procedure. Access to smaller, more peripheral lesions with a low risk of pneumothorax may also allow diagnosis of lung cancer at an earlier stage. However, current research is limited mostly to small, single-center and single-operator studies, with diagnostic yield estimates generally ranging between 59 and 94 %. In contrast, one recent registry reported a diagnostic yield rate of only 38.5 % in 39 cases using ENB guidance alone and 47.1 % in 266 cases using ENB combined with EBUS, with overall diagnostic yield ranging from 33 % to 73 % across the 10 included centers [29]. Thus, the full picture of how ENB procedures are used in clinical practice across diverse sites and geographies remains unclear. By providing a large, heterogeneous dataset, the NAVIGATE study will address several important knowledge gaps and provide data on the real-world use of ENB procedures.

Long-term data

Of the 24 published original studies on the use of ENB procedures to aid in the diagnosis of peripheral lung lesions presented in Table 1, fewer than half reported on patient outcomes beyond 1 year. Long-term data from the NAVIGATE study will elucidate the accuracy of ENB-aided diagnoses over time and provide valuable information on how that diagnosis and the stage of diagnosis may influence the patient’s treatment path.

New data

The 3 published meta-analyses currently available on ENB procedures all draw largely from the same dataset [3032]. NAVIGATE will provide an entirely unique dataset derived from a diverse patient population. Furthermore, because product versions and ancillary tools, as well as the way operators use those tools, are constantly evolving, NAVIGATE will provide an updated source of information that the medical community can use to evaluate this procedure to the present day. As technology progresses and new products are introduced, this will also be captured in NAVIGATE with the potential to examine the impact of technology iterations on performance.

Generalizable data

With an enrollment cap of 75 subjects per site, NAVIGATE will collect data from a diverse array of sites, user experience levels, and geographies. More importantly, the study allows complete independence regarding user preferences and diagnostic modalities. While all ancillary biopsy tools, complementary imaging methods, and follow-up procedures will be captured and reported, NAVIGATE does not mandate the use of any specific procedure. Rather, NAVIGATE is designed simply to evaluate the clinical use of the ENB procedure in the medical community. The eligibility criteria for enrollment into NAVIGATE are intentionally broad to allow an unrestricted assessment of how is ENB used in everyday clinical practice in accordance with current guidelines. In particular, while ENB is typically thought of as a tool for the evaluation of peripheral lesions, the profile of ENB use for peripheral versus central lesions, primary cancers versus metastatic disease, and operable versus inoperable patients is not well known. NAVIGATE is designed to capture that information and increase our understanding of the population of patients in whom ENB is used and what patient profile is most appropriate for the ENB procedure versus alternative methods. NAVIGATE will also evaluate the usage and utility of ENB-aided samples for genetic testing, according to local practice requirements. This will provide current information to determine the value of ENB in this constantly changing field of knowledge.

Standardized definitions

In addition to variations among user experience and patient characteristics, an important reason for the range in ENB-aided diagnostic yield across studies is simply the definition of diagnostic yield itself. Many studies lack clearly defined performance outcomes or differ in how indeterminate results are handled. NAVIGATE will use well-defined and widely accepted definitions of diagnostic yield, sensitivity, specificity, and negative and positive predictive value and evaluate the validity of those definitions across a large dataset.

NAVIGATE will also evaluate the validity of common definitions for pneumothorax and bronchopulmonary hemorrhage. In particular, because there is no internationally standardized scale to measure airway bleeding, NAVIGATE will pilot the use of a new scale developed by investigators in this study and validated by expert consensus (E. Folch and S. Khandhar, unpublished personal communication; publication in progress). This scale will be evaluated side-by-side with the internationally standardized and recognized CTCAE grading system [38]. Pneumothorax severity will also be evaluated by a newly validated expert consensus scale that takes into account variance in international standard of care for observation and intervention following asymptomatic pneumothorax and compared to the CTCAE criteria (E. Folch and S. Khandhar, unpublished personal communication).

Stage migration

Only 15 % of all lung cancers are diagnosed at a localized stage when the cancer is more amenable to surgical resection for curative intent, which is typically associated with the highest chance of long-term survival [2]. Diagnosis at an earlier stage also results in significant cost savings [46]. With the ability to reach smaller, more peripheral lesions, ENB procedures may theoretically enable diagnosis of lung cancer at an earlier stage. A retrospective review of 286 cases of non–small-cell lung cancer in a single center demonstrated that there was a greater proportion of early-stage diagnoses after the introduction of ENB compared to before the introduction of ENB [47]. NAVIGATE will prospectively assess stage at diagnosis and other associated procedures within the follow-up timeframe to confirm this result in a larger, multicenter dataset.

Healthcare utilization and economic profile

One criticism of ENB is that it is more time-consuming and expensive and requires more resources than other techniques [30]. However, other studies have reported that, despite higher acquisition cost, ENB procedures are slightly less expensive than TTNA due to higher complication costs with TTNA [48]. NAVIGATE will assess ENB costs, as well as downstream payments for follow-up procedures, to determine how ENB – and potentially an earlier diagnosis and lower pneumothorax rate – impacts long-term cost-effectiveness. NAVIGATE will also evaluate all healthcare services and procedures related to lung cancer diagnosis and treatment following the initial ENB index procedure through 2-year follow-up, for the purpose of defining the treatment pathway after the initial ENB-aided diagnosis.

Predicting the probability of malignancy

With recent discussions on the value of screening for lung cancer, the number of patients with positive CT findings is likely to increase, particularly with the recommendations for low-dose CT screening for high-risk individuals by joint societies (e.g., Centers for Medicare and Medicaid Services, Unites States Preventive Services Task Force, National Comprehensive Cancer Network, American College of Chest Physicians, Society of Thoracic Surgeons) [49]. Published studies have reported that approximately 25 % of patients who undergo low-dose CT screening will have a positive finding [3], with up to 50 % in smokers over the age of 50 [50]. The anxiety and stress that patients experience from a positive CT finding can be further compounded by the development of a complication during the diagnostic workup. In the NLST study, 8.2 %–11.2 % of patients diagnosed with lung cancer were associated with having a major complication after an invasive procedure [3]. Thus, there is an increasing need for appropriate tools and information to guide physicians on how to handle positive findings based on the clinical estimation of risk. The clinician must evaluate the overall probability of malignancy in order to determine which patients can be safely observed (<10 % probability of malignancy) and which require immediate excision (>90 % probability of malignancy). For moderately sized or indeterminate lesions, the appropriate course is often unclear. NAVIGATE will provide information on which approach (watchful waiting with serial CT scans, tissue biopsy, or direct excision) proves most effective over time based on pre-procedure probability of malignancy and ENB findings. NAVIGATE will also compare physician-estimated pre-procedure probability of malignancy to a mathematical model that calculates risk based on patient age, smoking history, history of extrathoracic malignancy, nodule size, nodule border characteristics, and nodule location [36, 37]. This calculation tool has been proven equivalent to other estimation tools, requires few data points, is easy to use, and is globally available. An ancillary objective of the NAVIGATE study is to validate this tool in a larger dataset and compare the long-term accuracy of the probability of malignancy based on this calculation compared to the clinician’s pre-procedure estimate.

Quality of life

Lung cancer patients are increasingly concerned with quality of life and loss of lung function following surgical resection. Physician and patient comfort levels and comorbidities must also be considered in every case. When warranted, minimally invasive diagnostic options may be preferred for patients with suspicious nodules and low probability of malignancy.

NAVIGATE will assess patient health status and quality of life using the EQ-5D-3 L questionnaire [39, 40], a standardized measure of health status over a 24-month period. In addition, assessments of patient satisfaction, healthcare utilization, and worker productivity will provide information on the impact of ENB on the continuum of care. Potential subgroup analyses might also examine how quality of life, patient satisfaction, and healthcare utilization differ based on the purpose of the original ENB procedure (e.g., primary tumor versus metastases, screening versus diagnosis, staging, marker placement, etc.) and the diagnosis.


NAVIGATE will have a substantial impact on both the pulmonology and thoracic surgery communities. With up to 2,500 subjects planned, NAVIGATE will be approximately 10 times larger than the largest ENB study to date. The intent of the study is to investigate real-world utilization patterns and outcomes in a broad range of both academic and community centers, including evaluations of diagnostic yield and accuracy and of success rates of fiducial marker placement, dye marking, and lymph node biopsies. Additionally, subgroup analyses are planned based on geography, patient demographics and medical history, investigator experience, and lesion and procedure characteristics. This study will answer questions that remain largely unexplored in a large multi-center trial and will provide a wealth of information to the medical community regarding the full profile of ENB usage. In addition, clinical utility and outcomes identified in NAVIGATE will be instructive for the design of future comparative studies.



computed tomography


common terminology criteria for adverse events


endobronchial ultrasound


electromagnetic navigation bronchoscopy


ENB productivity and activity questionnaire


transthoracic needle aspiration


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Study sponsored by Medtronic, which was involved in the design of the study and the decision to submit the manuscript for publication, in collaboration with the authors. Medical writing support was provided by Kristin L. Hood PhD (an employee of Medtronic and coauthor on this paper). The authors also wish to thank Ryan Van Wert and Gina Murray for their contributions to study design, Jennifer Wolvers (Medtronic) for contributions to study design and management, and Mei Jiang (Medtronic) for biostatistics support.


Study sponsored and funded by Medtronic (Minneapolis, MN). Related to the submitted work: EEF, MRB, TG, SDM, EMT, MMW, TW, and SJK serve on the Clinical Advisory Board for Medtronic and received travel funds and fees for participation; KH is a full-time employee of Medtronic; MMW received consulting fees from Medtronic; TW received speaker fees from Medtronic. Outside the submitted work: EEF is on the Scientific Advisory board for Boston Scientific and the Education Advisory Board for Olympus; MRB received consulting fees from Medtronic; EMT received travel funds and honoraria from Medtronic as a member of their Speakers’ Bureau; TW received a research grant form Veran Medical Systems.

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Correspondence to Erik E. Folch.

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Competing interests

Study sponsored and funded by Medtronic (Minneapolis, MN). Other competing interests related to the submitted work: EEF, MRB, TG, SDM, EMT, MMW, TW, and SJK serve on the Clinical Advisory Board for Medtronic and received travel funds and fees for participation; KH is a full-time employee of Medtronic; MMW received consulting fees from Medtronic; TW received speaker fees from Medtronic. Outside the submitted work: EEF is on the Scientific Advisory board for Boston Scientific and the Education Advisory Board for Olympus; MRB received consulting fees from Medtronic; EMT received travel funds and honoraria from Medtronic as a member of their Speakers’ Bureau; TW received a research grant form Veran Medical Systems.

Authors’ contributions

All authors qualify for authorship under the ICMJE Recommendations (, including: substantial contributions to conception and design (all authors), drafting the article (EF, SK, KH) or critical revisions of the article (all authors); and final approval of the version to be published (all authors).

Additional files

Additional file 1:

Activated Sites as of February 19, 2016. (PDF 42 kb)

Additional file 2:

Calculated Probability of Malignancy. (PDF 34 kb)

Additional file 3:

Peripheral Lung Lesion Definition. (PDF 91 kb)

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Folch, E.E., Bowling, M.R., Gildea, T. et al. Design of a prospective, multicenter, global, cohort study of electromagnetic navigation bronchoscopy. BMC Pulm Med 16, 60 (2016).

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  • Bronchoscopy
  • Electromagnetic navigation
  • Image-guided biopsy
  • Lung cancer
  • Lung neoplasms
  • Neoplasm staging
  • Solitary pulmonary nodule
  • superDimension