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Completed Phase 3 Interventional

Efficacy and Safety Comparison of Tiotropium Inhalation Solution (Respimat Inhaler) and Spiriva HandiHaler in COPD

ClinicalTrials.gov ID: NCT00239447

Public ClinicalTrials.gov record NCT00239447. 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 21, 2026, 12:07 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

Efficacy and Safety Comparison of 4-week Treatment Periods of Two Doses [5 μg (2 Actuations of 2.5 μg) and 10 μg (2 Actuations of 5 μg)] of Tiotropium Inhalation Solution Delivered by the Respimat Inhaler, Tiotropium Inhalation Powder Capsule (18μg) Delivered by the HandiHaler in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study identification

NCT ID
NCT00239447
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
131 participants

Conditions and interventions

Interventions

  • Tiotropium Drug
  • HandiHaler Device
  • Respimat SMI Device

Drug · 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
Nov 25, 2002
Primary completion
Apr 28, 2004
Completion
Apr 28, 2004
Last update posted
Nov 30, 2023

2002 – 2004

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Division of Pulmonary and Critical Care Medicine Little Rock Arkansas 72205
Boehringer Ingelheim Investigational Site San Diego California 92120
San Jose Clinical Research San Jose California 95128
Boehringer Ingelheim Investigational Site Stockton California 95207
National Jewish Medical and Research Center Denver Colorado 80206-2762
LSU MC-Sheveport Shreveport Louisiana 71103
Minisota Lung Center Minneapolis Minnesota 55407
Wake Forest University School of Medicine Winston-Salem North Carolina 27157
Spartanburg Medical Research Spartanburg South Carolina 29303
Boehringer Ingelheim Investigational Site Tacoma Washington 98405

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00239447, 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 Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00239447 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →