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Completed Phase 3 Interventional Results available

12 / 48 wk Pivotal PFT vs PBO in COPD II

ClinicalTrials.gov ID: NCT00782509

Public ClinicalTrials.gov record NCT00782509. 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 23, 2026, 6:23 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

Randomised, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Efficacy and Safety of 48 Weeks of Once Daily Treatment of Orally Inhaled BI 1744 CL (5 mcg [2 Actuations of 2.5 mcg] and 10 mcg [2 Actuations of 5 mcg]) Delivered by the Respimat® Inhaler, in Patients With Chronic Obstructive Pulmonary Disease (COPD

Study identification

NCT ID
NCT00782509
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
644 participants

Conditions and interventions

Interventions

  • Olodaterol (BI 1744) Drug
  • Placebo 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
Jan 31, 2009
Primary completion
Aug 31, 2010
Completion
Not listed
Last update posted
Jun 26, 2014

Started 2009

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
1222.12.1227 Boehringer Ingelheim Investigational Site Mobile Alabama
1222.12.1218 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
1222.12.1226 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
1222.12.1214 Boehringer Ingelheim Investigational Site Waterbury Connecticut
1222.12.1207 Boehringer Ingelheim Investigational Site Clearwater Florida
1222.12.1224 Boehringer Ingelheim Investigational Site Panama City Florida
1222.12.1222 Boehringer Ingelheim Investigational Site Tampa Florida
1222.12.1208 Boehringer Ingelheim Investigational Site Winter Park Florida
1222.12.1220 Boehringer Ingelheim Investigational Site River Forest Illinois
1222.12.1229 Boehringer Ingelheim Investigational Site New Orleans Louisiana
1222.12.1219 Boehringer Ingelheim Investigational Site Ann Arbor Michigan
1222.12.1209 Boehringer Ingelheim Investigational Site Livonia Michigan
1222.12.1233 Boehringer Ingelheim Investigational Site Henderson Nevada
1222.12.1228 Boehringer Ingelheim Investigational Site Summit New Jersey
1222.12.1206 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
1222.12.1205 Boehringer Ingelheim Investigational Site Rochester New York
1222.12.1213 Boehringer Ingelheim Investigational Site Elizabeth City North Carolina
1222.12.1223 Boehringer Ingelheim Investigational Site Harrisburg North Carolina
1222.12.1217 Boehringer Ingelheim Investigational Site Raleigh North Carolina
1222.12.1203 Boehringer Ingelheim Investigational Site Cincinnatti Ohio
1222.12.1201 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
1222.12.1230 Boehringer Ingelheim Investigational Site Easley South Carolina
1222.12.1216 Boehringer Ingelheim Investigational Site Greenville South Carolina
1222.12.1221 Boehringer Ingelheim Investigational Site Dallas Texas
1222.12.1212 Boehringer Ingelheim Investigational Site Danville Virginia
1222.12.1211 Boehringer Ingelheim Investigational Site Richmond Virginia
1222.12.1225 Boehringer Ingelheim Investigational Site Richmond Virginia
1222.12.1232 Boehringer Ingelheim Investigational Site Morgantown West 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 23 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00782509, 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 Jun 26, 2014 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00782509 live on ClinicalTrials.gov.

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