Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Characterisation of 24-hour FEV1-time Profiles of Inhaled BI 1744 CL and Inhaled Foradil in Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT00932646

Public ClinicalTrials.gov record NCT00932646. 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 22, 2026, 6:21 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

Characterization of 24 Hour Spirometry Profiles of Inhaled BI 1744 CL and Inhaled Foradil in Patients With Chronic Obstructive Pulmonary Disease

Study identification

NCT ID
NCT00932646
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

  • BI 1744 (Olodaterol) Low Dose Drug
  • BI 1744 (Olodaterol) Medium Dose Drug
  • Placebo Drug
  • Foradil 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
May 31, 2009
Primary completion
Apr 30, 2010
Completion
Not listed
Last update posted
Feb 4, 2016

Started 2009

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
1222.25.25009 Boehringer Ingelheim Investigational Site Jasper Alabama
1222.25.25002 Boehringer Ingelheim Investigational Site Clearwater Florida
1222.25.25003 Boehringer Ingelheim Investigational Site DeLand Florida
1222.25.25007 Boehringer Ingelheim Investigational Site Winter Park Florida
1222.25.25010 Boehringer Ingelheim Investigational Site Austell Georgia
1222.25.25008 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
1222.25.25012 Boehringer Ingelheim Investigational Site Charlotte North Carolina
1222.25.25004 Boehringer Ingelheim Investigational Site Raleigh North Carolina
1222.25.25011 Boehringer Ingelheim Investigational Site Columbus Ohio
1222.25.25014 Boehringer Ingelheim Investigational Site Seneca South Carolina
1222.25.25006 Boehringer Ingelheim Investigational Site Knoxville Tennessee
1222.25.25005 Boehringer Ingelheim Investigational Site Houston Texas
1222.25.25013 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00932646, 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 Feb 4, 2016 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00932646 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →