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Completed Phase 3 Interventional Results available

Combivent Respimat 1-year Safety Study in Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT01019694

Public ClinicalTrials.gov record NCT01019694. 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 24, 2026, 12:27 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

Patient Acceptability of Ipratropium Bromide/Albuteroll Delivered by the Respimat® Inhaler in Adults With Chronic Obstructive Pulmonary Disease

Study identification

NCT ID
NCT01019694
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
470 participants

Conditions and interventions

Interventions

  • Combivent CFC-MDI Drug
  • Combivent Respimat 20/100 mcg Drug
  • Atrovent HFA 42 mcg + Albuterol HFA 200 mcg 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
Oct 31, 2009
Primary completion
Mar 31, 2011
Completion
Not listed
Last update posted
Oct 22, 2014

Started 2009

United States locations

U.S. sites
55
U.S. states
26
U.S. cities
50
Facility City State ZIP Site status
1012.62.153 Boehringer Ingelheim Investigational Site Jasper Alabama
1012.62.145 Boehringer Ingelheim Investigational Site Mobile Alabama
1012.62.156 Boehringer Ingelheim Investigational Site Mesa Arizona
1012.62.135 Boehringer Ingelheim Investigational Site Berkeley California
1012.62.141 Boehringer Ingelheim Investigational Site Riverside California
1012.62.155 Boehringer Ingelheim Investigational Site Boulder Colorado
1012.62.126 Boehringer Ingelheim Investigational Site Fort Collins Colorado
1012.62.131 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
1012.62.144 Boehringer Ingelheim Investigational Site Stamford Connecticut
1012.62.123 Boehringer Ingelheim Investigational Site Waterbury Connecticut
1012.62.114 Boehringer Ingelheim Investigational Site Clearwater Florida
1012.62.124 Boehringer Ingelheim Investigational Site DeLand Florida
1012.62.139 Boehringer Ingelheim Investigational Site Pensacola Florida
1012.62.134 Boehringer Ingelheim Investigational Site Tampa Florida
1012.62.115 Boehringer Ingelheim Investigational Site Winter Park Florida
1012.62.146 Boehringer Ingelheim Investigational Site Decatur Georgia
1012.62.113 Boehringer Ingelheim Investigational Site Coeur d'Alene Idaho
1012.62.157 Boehringer Ingelheim Investigational Site Dubuque Iowa
1012.62.159 Boehringer Ingelheim Investigational Site Louisville Kentucky
1012.62.116 Boehringer Ingelheim Investigational Site Lafayette Louisiana
1012.62.148 Boehringer Ingelheim Investigational Site New Orleans Louisiana
1012.62.137 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts
1012.62.132 Boehringer Ingelheim Investigational Site Ann Arbor Michigan
1012.62.117 Boehringer Ingelheim Investigational Site Livonia Michigan
1012.62.158 Boehringer Ingelheim Investigational Site Minneapolis Minnesota
1012.62.127 Boehringer Ingelheim Investigational Site St Louis Missouri
1012.62.129 Boehringer Ingelheim Investigational Site St Louis Missouri
1012.62.147 Boehringer Ingelheim Investigational Site Cherry Hill New Jersey
1012.62.149 Boehringer Ingelheim Investigational Site Summit New Jersey
1012.62.112 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
1012.62.111 Boehringer Ingelheim Investigational Site Rochester New York
1012.62.107 Boehringer Ingelheim Investigational Site Cincinnati Ohio
1012.62.120 Boehringer Ingelheim Investigational Site Cincinnati Ohio
1012.62.150 Boehringer Ingelheim Investigational Site Toledo Ohio
1012.62.103 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1012.62.104 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
1012.62.154 Boehringer Ingelheim Investigational Site East Providence Rhode Island
1012.62.128 Boehringer Ingelheim Investigational Site Charleston South Carolina
1012.62.130 Boehringer Ingelheim Investigational Site Easley South Carolina
1012.62.151 Boehringer Ingelheim Investigational Site Greenville South Carolina
1012.62.161 Boehringer Ingelheim Investigational Site Greenville South Carolina
1012.62.109 Boehringer Ingelheim Investigational Site Greer South Carolina
1012.62.118 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
1012.62.125 Boehringer Ingelheim Investigational Site Austin Texas
1012.62.140 Boehringer Ingelheim Investigational Site Fort Worth Texas
1012.62.143 Boehringer Ingelheim Investigational Site Houston Texas
1012.62.152 Boehringer Ingelheim Investigational Site Killeen Texas
1012.62.102 Boehringer Ingelheim Investigational Site San Antonio Texas
1012.62.122 Boehringer Ingelheim Investigational Site Danville Virginia
1012.62.119 Boehringer Ingelheim Investigational Site Richmond Virginia
1012.62.142 Boehringer Ingelheim Investigational Site Richmond Virginia
1012.62.108 Boehringer Ingelheim Investigational Site Spokane Washington
1012.62.133 Boehringer Ingelheim Investigational Site Spokane Washington
1012.62.105 Boehringer Ingelheim Investigational Site Tacoma Washington
1012.62.101 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01019694, 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 Oct 22, 2014 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01019694 live on ClinicalTrials.gov.

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