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Table 2 Changes from baseline in lung function and body plethysmography parameters at Week 3 (ITT population)

From: Aclidinium improves exercise endurance, dyspnea, lung hyperinflation, and physical activity in patients with COPD: a randomized, placebo-controlled, crossover trial

Parameter

Placebo (N = 108)

Aclidinium 400 μg BID (N = 109)

Treatment difference vs placebo (95% CI)

Pre-dose (trough) IC (mL)

20 (25)

98 (24)

78 (10, 145)*

Pre-dose (trough) FEV1 (mL)

-25 (21)

108 (21)

132 (74, 191)****

Pre-dose (trough) FVC (mL)

-46 (31)

198 (30)

243 (157, 329)****

FRC (mL)

   

 Pre-dose (trough)

15 (39)

-182 (39)

-197 (-321, -72)**

 Post-dose

-130 (46)

-449 (46)

-318 (-448, -189)****

RV (mL)

   

 Pre-dose (trough)

15 (60)

-222 (60)

-238 (-396, -79)**

 Post-dose

-81 (57)

-523 (57)

-443 (-599, -286)****

TLC (mL)

   

 Pre-dose (trough)

-6 (41)

-82 (41)

-76 (-201, 49)

 Post-dose

-49 (41)

-199 (41)

-150 (-262, -37)**

sGaw (s-1kPa-1)

   

 Pre-dose (trough)

0.002 (0.020)

0.096 (0.020)

0.094 (0.038, 0.150)**

 Post-dose

0.054 (0.027)

0.297 (0.026)

0.243 (0.182, 0.303)****

  1. Data reported as least squares means (standard error) change from baseline (analysis of covariance).
  2. *p < 0.05, **p < 0.01, ****p < 0.0001 versus placebo.
  3. BID, twice daily; CI, confidence interval; FEV1, forced expiratory volume in 1 s; FRC, functional residual capacity; FVC, forced vital capacity; IC, inspiratory capacity; ITT, intent-to-treat; RV, residual volume; sGaw, specific airway conductance; TLC, total lung capacity.