drugset / Trial / NCT00168831

Tiotropium / Respimat One-Year Study

NCT00168831 ↗

Phase 3 Completed 1007 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the long term effects of treatment with two doses of Tiotropium delivered by the Respimat inhaler in patients with COPD.

Timeline

Start
2003-02
Primary completion
2005-06
Completion
—

Outcome

Met primary endpoint

registry analysis (superiority or other test); Tiotropium Respimat 5mcg vs Placebo; p <0.0001; Mean Difference (Final Values) 0.113; ANCOVA NCT00168831 ↗

registry analysis (superiority or other test); Tiotropium Respimat 5mcg vs Placebo; p = 0.0004; Mean Difference (Final Values) -3.713; ANCOVA NCT00168831 ↗

registry analysis (superiority or other test); Tiotropium Respimat 5mcg vs Placebo; p <0.0001; Mean Difference (Final Values) 1.053; ANCOVA NCT00168831 ↗

registry analysis (superiority or other test); Tiotropium Respimat 5mcg vs Placebo; p = 0.0002; Odds Ratio (OR) 0.782 (95% CI 0.687 to 0.890); Poisson regression NCT00168831 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tiotropium Other / unclassified 5 ug Inhaled
Subject Tiotropium Other / unclassified 10 ug Inhaled