Clinical trial

12 Week Comparison of 5 Mcg and 10 Mcg of Tiotropium / Respimat, Placebo and…

NCT00239473 · Boehringer Ingelheim, Industry · Completed

Key facts

NCT number NCT00239473
Title 12 Week Comparison of 5 Mcg and 10 Mcg of Tiotropium / Respimat, Placebo and Ipratropium MDI in COPD
Official title A Randomised, Double-Blind, Double-Dummy, Placebo- and Active-Controlled, Parallel Group Efficacy and Safety Comparison of 12-Week Treatment of Two Doses [5 μg (2 Actuations of 2.5 μg) and 10 μg (2 Actuations of 5 μg)] of Tiotropium Inhalation Solution Delivered by the Respimat Inhaler, Placebo and…
Lead sponsor Boehringer Ingelheim, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Pulmonary Disease, Chronic Obstructive
Intervention type Device
Interventions 5 mcg once daily tiotropium inhalation solution delivered by the Respimat inhaler, 10 mcg once daily tiotropium inhalation solution delivered by the Respimat inhaler
Enrollment 429
Start date Nov 1, 2002
Primary completion Dec 1, 2003
First posted Oct 17, 2005
Last update posted Nov 1, 2013
Countries Germany, Italy, South Africa, Switzerland

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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