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Table 2 Basic information of 5 RCTs

From: Efficacy of N-acetylcysteine plus pirfenidone in the treatment of idiopathic pulmonary fibrosis: a systematic review and meta-analysis

Reference

Location

Study Design

Date of Trial

TG/CG (n)

Age (years, TG/CG)

TG(NACā€‰+ā€‰PFD,mg/d)

CG(PFD,mg/d)

Duration of Treatment

Outcomes

Sakamoto (2021) [18]

Japan

M,RCT

Jun 2015ā€”Jun 2018

34/36

71.0ā€‰Ā±ā€‰7.3/73.3ā€‰Ā±ā€‰7.0

704.8 (inhaled)ā€‰+ā€‰1200ā€“1800

1200ā€“1800

48 weeks

ā‘ ā‘¤ā‘„ā‘¦ā‘§ā‘Ø

Behr (2016) [19]

Europe (8 countries)

M,DB,RCT

Jun 2013ā€”Feb 2015

60/62

66Ā·7ā€‰Ā±ā€‰8.0/66Ā·7ā€‰Ā±ā€‰6.2

1800ā€‰+ā€‰1602ā€“2403

1602ā€“2403ā€‰+ā€‰placebo

24 weeks

ā‘ ā‘”ā‘¢ā‘£ā‘¤ā‘„ā‘¦ā‘§ā‘Ø

Wen (2019) [22]

China

RCT

Nov 2012ā€”Nov 2015

43/43

56.24ā€‰Ā±ā€‰10.2/55.63ā€‰Ā±ā€‰10.54

1800ā€‰+ā€‰1200

1200

6 month

ā‘ ā‘£ā‘„ā‘Ø

Zhou (2021) [23]

China

RCT

Jan 2018ā€”Jan 2020

38/40

65.81ā€‰Ā±ā€‰8.76/66.45ā€‰Ā±ā€‰9.23

1800ā€‰+ā€‰600ā€“1800

600ā€“18

6 month

ā‘ ā‘¤ā‘„ā‘¦ā‘§ā‘Ø

Zhao (2023) [24]

China

RCT

Mar 2019ā€”Mar 2022

21/21

64.3ā€‰Ā±ā€‰9.2/61.1ā€‰Ā±ā€‰8.8

600(inhaled)ā€‰+ā€‰600ā€“1800

600ā€“1800

24 weeks

ā‘ ā‘¢ā‘£ā‘¤ā‘„ā‘¦ā‘§ā‘Ø

  1. CCT Caseā€“control trial, CS Cohort study, RCT Randomized controlled trial, NAC N-acetylcysteine, PFD Pirfenidone, M Multicenter, DB Double-blind, CG Control group, TG Treatment group
  2. ā‘  Ī”FVC Changes in forced vital capacity
  3. ā‘” Ī”FVC% Changes in forced vital capacity percent predicted
  4. ā‘¢ Ī”6MWT Changes in 6-min walking test distance
  5. ā‘£ Ī”DLco% Changes in percentage of predicted carbon monoxide diffusing capacity
  6. ā‘¤ At least one side effects
  7. ā‘„ Severe side effects
  8. ā‘¦ Gastrointestinal effects
  9. ā‘§ Skin side effects
  10. ā‘Ø Mortality rate