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Completed Phase 3 Interventional Results available

Respimat® Combivent Trial in Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT00400153

Public ClinicalTrials.gov record NCT00400153. 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 Sep 1, 2026, 8:42 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

Safety and Efficacy of Combivent Respimat in Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to compare the effect of ipratropium bromide/salbutamol inhalation spray combination administered by the Respimat® inhaler (20 mcg/100 mcg), ipratropium bromide inhalation spray administered by the Respimat® inhaler (20 mcg), and COMBIVENT® MDI administered q.i.d on FEV1 at intervals over a treatment period of 12 weeks in patients with COPD. Specifically, non-inferiority of Combivent Respimat® to COMBIVENT® MDI in FEV1 AUC from 0 to 6 hours , superiority of Combivent Respimat® to Atrovent Respimat® monotherapy in FEV1 AUC from 0 to 4 hours, and non-inferiority of Combivent Respimat® to Atrovent Respimat® monotherapy in FEV1 AUC from 4 to 6 hours will be analyzed. In addition, steady state pharmacokinetics over one dosing interval following 4 weeks of therapy will be characterized in a subgroup of patients.

Study identification

NCT ID
NCT00400153
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
1,480 participants

Conditions and interventions

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 31, 2006
Primary completion
Mar 31, 2008
Completion
Not listed
Last update posted
Jun 12, 2014

Started 2006

United States locations

U.S. sites
87
U.S. states
31
U.S. cities
77
Facility City State ZIP Site status
1012.56.01006 Boehringer Ingelheim Investigational Site Birmingham Alabama
1012.56.01051 Boehringer Ingelheim Investigational Site Jasper Alabama
1012.56.01071 Boehringer Ingelheim Investigational Site Mobile Alabama
1012.56.01039 Boehringer Ingelheim Investigational Site Phoenix Arizona
1012.56.01012 Boehringer Ingelheim Investigational Site Lakewood California
1012.56.01029 Boehringer Ingelheim Investigational Site Los Angeles California
1012.56.01043 Boehringer Ingelheim Investigational Site Palo Alto California
1012.56.01089 Boehringer Ingelheim Investigational Site Rancho Mirage California
1012.56.01021 Boehringer Ingelheim Investigational Site Riverside California
1012.56.01033 Boehringer Ingelheim Investigational Site San Jose California
1012.56.01020 Boehringer Ingelheim Investigational Site Sepulveda California
1012.56.01045 Boehringer Ingelheim Investigational Site Torrence California
1012.56.01040 Boehringer Ingelheim Investigational Site Denver Colorado
1012.56.01050 Boehringer Ingelheim Investigational Site Fort Collins Colorado
1012.56.01018 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
1012.56.01062 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
1012.56.01036 Boehringer Ingelheim Investigational Site Hartford Connecticut
1012.56.01025 Boehringer Ingelheim Investigational Site Stamford Connecticut
1012.56.01088 Boehringer Ingelheim Investigational Site Waterbury Connecticut
1012.56.01007 Boehringer Ingelheim Investigational Site Bay Pines Florida
1012.56.01058 Boehringer Ingelheim Investigational Site Brandon Florida
1012.56.01010 Boehringer Ingelheim Investigational Site Clearwater Florida
1012.56.01065 Boehringer Ingelheim Investigational Site Clearwater Florida
1012.56.01024 Boehringer Ingelheim Investigational Site DeLand Florida
1012.56.01001 Boehringer Ingelheim Investigational Site Melbourne Florida
1012.56.01023 Boehringer Ingelheim Investigational Site Panama City Florida
1012.56.01052 Boehringer Ingelheim Investigational Site Pensecola Florida
1012.56.01048 Boehringer Ingelheim Investigational Site Tampa Florida
1012.56.01093 Boehringer Ingelheim Investigational Site Winter Park Florida
1012.56.01077 Boehringer Ingelheim Investigational Site Atlanta Georgia
1012.56.01083 Boehringer Ingelheim Investigational Site Decatur Georgia
1012.56.01008 Boehringer Ingelheim Investigational Site Coeur d'Alene Idaho
1012.56.01019 Boehringer Ingelheim Investigational Site Olathe Kansas
1012.56.01056 Boehringer Ingelheim Investigational Site Wichita Kansas
1012.56.01066 Boehringer Ingelheim Investigational Site Bowling Green Kentucky
1012.56.01090 Boehringer Ingelheim Investigational Site Lafayette Louisiana
1012.56.01054 Boehringer Ingelheim Investigational Site New Orleans Louisiana
1012.56.01072 Boehringer Ingelheim Investigational Site New Orleans Louisiana
1012.56.01070 Boehringer Ingelheim Investigational Site Shreveport Louisiana
1012.56.01035 Boehringer Ingelheim Investigational Site Baltimore Maryland
1012.56.01079 Boehringer Ingelheim Investigational Site Ann Arbor Michigan
1012.56.01044 Boehringer Ingelheim Investigational Site Minneapolis Minnesota
1012.56.01076 Boehringer Ingelheim Investigational Site St Louis Missouri
1012.56.01082 Boehringer Ingelheim Investigational Site Henderson Nevada
1012.56.01049 Boehringer Ingelheim Investigational Site Reno Nevada
1012.56.01080 Boehringer Ingelheim Investigational Site Brick New Jersey
1012.56.01027 Boehringer Ingelheim Investigational Site Cherry Hill New Jersey
1012.56.01028 Boehringer Ingelheim Investigational Site Summit New Jersey
1012.56.01069 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
1012.56.01022 Boehringer Ingelheim Investigational Site Larchmont New York
1012.56.01015 Boehringer Ingelheim Investigational Site New Hyde Park New York
1012.56.01068 Boehringer Ingelheim Investigational Site New York New York
1012.56.01078 Boehringer Ingelheim Investigational Site Asheville North Carolina
1012.56.01017 Boehringer Ingelheim Investigational Site Raleigh North Carolina
1012.56.01042 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina
1012.56.01034 Boehringer Ingelheim Investigational Site Sylvania Ohio
1012.56.01031 Boehringer Ingelheim Investigational Site Toledo Ohio
1012.56.01038 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
1012.56.01016 Boehringer Ingelheim Investigational Site Medford Oregon
1012.56.01067 Boehringer Ingelheim Investigational Site Hershey Pennsylvania
1012.56.01003 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1012.56.01060 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1012.56.01004 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
1012.56.01087 Boehringer Ingelheim Investigational Site East Providence Rhode Island
1012.56.01057 Boehringer Ingelheim Investigational Site Johnston Rhode Island
1012.56.01026 Boehringer Ingelheim Investigational Site Charleston South Carolina
1012.56.01037 Boehringer Ingelheim Investigational Site Charleston South Carolina
1012.56.01081 Boehringer Ingelheim Investigational Site Greenville South Carolina
1012.56.01085 Boehringer Ingelheim Investigational Site Greenville South Carolina
1012.56.01084 Boehringer Ingelheim Investigational Site Greer South Carolina
1012.56.01011 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
1012.56.01073 Boehringer Ingelheim Investigational Site Nashville Tennessee
1012.56.01075 Boehringer Ingelheim Investigational Site Nashville Tennessee
1012.56.01047 Boehringer Ingelheim Investigational Site Fort Worth Texas
1012.56.01014 Boehringer Ingelheim Investigational Site Houston Texas
1012.56.01032 Boehringer Ingelheim Investigational Site Killeen Texas
1012.56.01002 Boehringer Ingelheim Investigational Site San Antonio Texas
1012.56.01053 Boehringer Ingelheim Investigational Site San Antonio Texas
1012.56.01009 Boehringer Ingelheim Investigational Site Richmond Virginia
1012.56.01013 Boehringer Ingelheim Investigational Site Richmond Virginia
1012.56.01059 Boehringer Ingelheim Investigational Site Roanoke Virginia
1012.56.01055 Boehringer Ingelheim Investigational Site Salem Virginia
1012.56.01063 Boehringer Ingelheim Investigational Site Bellington Washington
1012.56.01005 Boehringer Ingelheim Investigational Site Spokane Washington
1012.56.01064 Boehringer Ingelheim Investigational Site Spokane Washington
1012.56.01030 Boehringer Ingelheim Investigational Site Tacoma Washington
1012.56.01074 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 93 non-U.S. sites.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00400153, 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 12, 2014 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00400153 live on ClinicalTrials.gov.

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