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Completed Phase 4 Interventional Results available

Tiotropium In Exercise

ClinicalTrials.gov ID: NCT00525512

Public ClinicalTrials.gov record NCT00525512. 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 Sep 1, 2026, 11:15 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 Two-year Trial to Examine the Changes in Exercise Endurance and COPD Treated With Tiotropium Once Daily (EXACTT)

Brief summary

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

The objective of this study is to evaluate the effects on exercise duration of 96 weeks treatment with 18 mcg tiotropium (Spiriva HandiHaler) daily as compared to placebo, in patients with COPD.

Study identification

NCT ID
NCT00525512
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
519 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
Jul 31, 2007
Primary completion
May 31, 2010
Completion
Not listed
Last update posted
Dec 23, 2013

Started 2007

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
205.368.01023 Boehringer Ingelheim Investigational Site Jasper Alabama
205.368.01022 Boehringer Ingelheim Investigational Site Phoenix Arizona
205.368.01003 Boehringer Ingelheim Investigational Site Los Angeles California
205.368.01008 Boehringer Ingelheim Investigational Site Fort Collins Colorado
205.368.01017 Boehringer Ingelheim Investigational Site Hartford Connecticut
205.368.01028 Boehringer Ingelheim Investigational Site Waterbury Connecticut
205.368.01004 Boehringer Ingelheim Investigational Site Bay Pines Florida
205.368.01013 Boehringer Ingelheim Investigational Site North Miami Beach Florida
205.368.01025 Boehringer Ingelheim Investigational Site Hazard Kentucky
205.368.01029 Boehringer Ingelheim Investigational Site Biddeford Maine
205.368.01016 Boehringer Ingelheim Investigational Site Baltimore Maryland
205.368.01002 Boehringer Ingelheim Investigational Site Boston Massachusetts
205.368.01021 Boehringer Ingelheim Investigational Site Kansas City Missouri
205.368.01014 Boehringer Ingelheim Investigational Site Albany New York
205.368.01030 Boehringer Ingelheim Investigational Site Tulsa Oklahoma
205.368.01018 Boehringer Ingelheim Investigational Site Charleston South Carolina
205.368.01027 Boehringer Ingelheim Investigational Site Gaffney South Carolina
205.368.01019 Boehringer Ingelheim Investigational Site Greenville South Carolina
205.368.01020 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
205.368.01024 Boehringer Ingelheim Investigational Site Union South Carolina
205.368.01015 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 41 non-U.S. sites.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00525512, 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 Dec 23, 2013 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00525512 live on ClinicalTrials.gov.

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