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Completed Phase 4 Interventional

Trial Comparing Treatment With Tiotropium Inhalation Capsules to Combivent® Inhalation Aerosol in COPD Patients.

ClinicalTrials.gov ID: NCT00388882

Public ClinicalTrials.gov record NCT00388882. 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, 12:48 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, Parallel Group Trial Comparing 12 Weeks Treatment With Tiotropium Inhalation Capsules 18 mcg Via the HandiHaler® Once Daily to Combivent® Inhalation Aerosol CFC MDI 2 Actuations q.i.d. in COPD Patients Currently Prescribed Combivent® Inhalation Aerosol CFC MDI

Study identification

NCT ID
NCT00388882
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
327 participants

Conditions and interventions

Interventions

  • tiotropium Drug
  • ipratropium bromide / albuterol 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
Oct 3, 2006
Primary completion
Oct 7, 2007
Completion
Not listed
Last update posted
Nov 30, 2023

Started 2006

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
205.346.107 Boehringer Ingelheim Investigational Site Phoenix Arizona
205.346.104 Boehringer Ingelheim Investigational Site Lakewood California
205.346.108 Boehringer Ingelheim Investigational Site Sepulveda California
205.346.101 Boehringer Ingelheim Investigational Site Torrance California
205.346.106 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
205.346.102 Boehringer Ingelheim Investigational Site Coeur d'Alene Idaho
205.346.109 Boehringer Ingelheim Investigational Site Shreveport Louisiana
205.346.110 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
205.346.105 Boehringer Ingelheim Investigational Site Charleston South Carolina
205.346.103 Boehringer Ingelheim Investigational Site Spartanburg South Carolina

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 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00388882, 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 30, 2023 · Synced Jun 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00388882 live on ClinicalTrials.gov.

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