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Completed Phase 3 Interventional Results available

Evaluation of Tiotropium 5 µg/Day Delivered Via the Respimat® Inhaler Over 48 Weeks in Patients With Severe Persistent Asthma on Top of Usual Care (Study I)

ClinicalTrials.gov ID: NCT00772538

Public ClinicalTrials.gov record NCT00772538. 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 May 12, 2026, 10:08 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 Phase III Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate Efficacy and Safety of Tiotropium Inhalation Solution Delivered Via Respimat® Inhaler (5 mcg/Day) Over 48 Weeks as add-on Controller Therapy on Top of Usual Care in Patients With Severe Persistent Asthma

Study identification

NCT ID
NCT00772538
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
459 participants

Conditions and interventions

Conditions

Interventions

  • placebo Drug
  • tiotropium 5mcg/day Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Sep 30, 2008
Primary completion
Jun 30, 2011
Completion
Not listed
Last update posted
Aug 17, 2014

Started 2008

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
205.416.01007 Boehringer Ingelheim Investigational Site Birmingham Alabama
205.416.01012 Boehringer Ingelheim Investigational Site Los Angeles California
205.416.01018 Boehringer Ingelheim Investigational Site Los Angeles California
205.416.01016 Boehringer Ingelheim Investigational Site Riverside California
205.416.01008 Boehringer Ingelheim Investigational Site San Diego California
205.416.01004 Boehringer Ingelheim Investigational Site Walnut Creek California
205.416.01010 Boehringer Ingelheim Investigational Site Stamford Connecticut
205.416.01023 Boehringer Ingelheim Investigational Site Tallahassee Florida
205.416.01002 Boehringer Ingelheim Investigational Site Elk Grove Village Illinois
205.416.01003 Boehringer Ingelheim Investigational Site Lexington Kentucky
205.416.01014 Boehringer Ingelheim Investigational Site Wheaton Maryland
205.416.01025 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts
205.416.01022 Boehringer Ingelheim Investigational Site Columbia Missouri
205.416.01021 Boehringer Ingelheim Investigational Site Boys Town Nebraska
205.416.01011 Boehringer Ingelheim Investigational Site Cherry Hill New Jersey
205.416.01001 Boehringer Ingelheim Investigational Site Cincinnati Ohio
205.416.01024 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
205.416.01017 Boehringer Ingelheim Investigational Site Lake Oswego Oregon
205.416.01019 Boehringer Ingelheim Investigational Site El Paso Texas
205.416.01009 Boehringer Ingelheim Investigational Site Richmond Virginia

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00772538, 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 Aug 17, 2014 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00772538 live on ClinicalTrials.gov.

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