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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 Jun 28, 2026, 12:43 AM 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

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

Interventions

  • 5 mcg once daily tiotropium inhalation solution delivered by the Respimat inhaler Device
  • 10 mcg once daily tiotropium inhalation solution delivered by the Respimat inhaler Device

Device

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
Oct 31, 2002
Primary completion
Nov 30, 2003
Completion
Not listed
Last update posted
Oct 31, 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 Oct 31, 2013 · Synced Jun 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00240435 live on ClinicalTrials.gov.

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