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Completed Phase 3 Interventional

Tiotropium (Spiriva) Rehabilitation Study

ClinicalTrials.gov ID: NCT00274521

Public ClinicalTrials.gov record NCT00274521. 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 Jul 24, 2026, 3:30 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, Placebo Controlled 25-week Trial to Compare the Effect of Tiotropium Inhalation Capsuled (18 Mcg) Once Daily on Exercise Tolerance in Patients With Chronic Obstructive Pulmonary Disease (COPD) Participating in 8 Weeks of Pulmonary Rehabilitation.

Study identification

NCT ID
NCT00274521
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
108 participants

Conditions and interventions

Interventions

  • Tiotropium Drug

Drug

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
Apr 30, 2001
Primary completion
Jan 31, 2003
Completion
Not listed
Last update posted
Oct 31, 2013

Started 2001

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama
Boehringer Ingelheim Investigational Site Phoenix Arizona
Attention: John E. Hodgkin, M.D. Deer Park California
Boehringer Ingelheim Investigational Site Long Beach California
UCLA School of Medicine Los Angeles California
Boehringer Ingelheim Investigational Site San Diego California
Harbor-UCLA Research and Education Institute Torrance California
Boehringer Ingelheim Investigational Site Fort Collins Colorado
Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
Boehringer Ingelheim Investigational Site Danbury Connecticut
St. Francis Hospital and Medical Center Hartford Connecticut
Norwalk Hospital Norwalk Connecticut
Boehringer Ingelheim Investigational Site Elk Grove Village Illinois
UMass Memorial Medical Center North Worcester Massachusetts
Henry Ford Hospital Detroit Michigan
University of Nebraska Medical Center Omaha Nebraska
Duke University Medical Center Durhan North Carolina
Temple University Hospital Philadelphia Pennsylvania
Boehringer Ingelheim Investigational Site Everett Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00274521, 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 Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00274521 live on ClinicalTrials.gov.

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