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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 Oct 28, 2026, 6:46 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, 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.

Brief summary

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

The study was designed to determine whether tiotropium inhalation capsules, compared to placebo, enhances the improvement in exercise tolerance seen in patients with chronic obstructive pulmonary disease (COPD) who participate in pulmonary rehabilitation. In addition, assessments of the effect of tiotropium on dyspnea and quality of life following pulmonary rehabilitation were taken.

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

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
May 2001 (Type not available)
Primary completion
Feb 2003 (Actual)
Completion
Not listed
Last update posted
Nov 1, 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 Nov 1, 2013 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00274521 live on ClinicalTrials.gov.

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