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Completed Phase 3 Interventional

12 Week Comparison of 5 Mcg and 10 Mcg of Tiotropium / Respimat, Placebo and Ipratropium MDI in COPD

ClinicalTrials.gov ID: NCT00240435

Public ClinicalTrials.gov record NCT00240435. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 2:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Double-dummy, Placebo- and Active-controlled, Parallel Group Efficacy and Safety Comparison of 12-week Treatment of Two Doses (5 Mcg and 10 Mcg) of Tiotropium Inhalation Solution Delivered by the Respimat Inhaler, Placebo and Ipratropium Bromide Inhalation Aerosol (MDI) i

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective was to compare the bronchodilator efficacy of two doses (5 mcg and 10 mcg) of tiotropium inhalation solution delivered by the Respimat inhaler once daily to placebo and to ipratropium bromide MDI four times daily in patients with COPD. The secondary objective was to compare the safety of tiotropium inhalation solution delivered by the Respimat to placebo and ipratropium bromide MDI.

Study identification

NCT ID
NCT00240435
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
491 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2002 (Type not available)
Primary completion
Dec 2003 (Actual)
Completion
Not listed
Last update posted
Nov 1, 2013

Started 2002

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Boehringer Ingelheim Investigational Site Birmingham Alabama — —
Boehringer Ingelheim Investigational Site Downey California — —
University of California - Los Angeles Los Angeles California — —
Boehringer Ingelheim Investigational Site Palo Alto California — —
Rocky Mountain Center for Clinical Research Wheat Ridge Colorado — —
Boehringer Ingelheim Investigational Site Bay Pines Florida — —
Boehringer Ingelheim Investigational Site Clearwater Florida — —
Boehringer Ingelheim Investigational Site Pembroke Pines Florida — —
Boehringer Ingelheim Investigational Site Wheaton Maryland — —
Boehringer Ingelheim Investigational Site St Louis Missouri — —
Boehringer Ingelheim Investigational Site New Hyde Park New York — —
Boehringer Ingelheim Investigational Site Elizabeth City North Carolina — —
Boehringer Ingelheim Investigational Site Charleston South Carolina — —
Boehringer Ingelheim Investigational Site Dallas Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00240435, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 1, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00240435 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →