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Completed Phase 3 Interventional

A Phase IIIB Study to Compare the Efficacy and Safety of Concomitant Treatment in Patients With COPD

ClinicalTrials.gov ID: NCT00308191

Public ClinicalTrials.gov record NCT00308191. 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 Oct 17, 2026, 3:20 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 6-Week Double-Blind, Parallel-Group, Active-Controlled Trial to Compare the Efficacy and Safety of Concomitant Treatment of Formoterol Fumarate Inhalation Solution 20 Mcg Twice Daily and Tiotropium 18 Mcg Once Daily to Tiotropium 18 Mcg Once Daily Alone in the Treatment of Patients With Chronic Obstructive Pulmonary Disease

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of the concomitant treatment of formoterol fumarate with tiotropium bromide compared to treatment with tiotropium bromide alone.

Study identification

NCT ID
NCT00308191
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Dey
Industry
Enrollment
128 participants

Conditions and interventions

Conditions

Interventions

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
Apr 2006 (Type not available)
Primary completion
May 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Mar 7, 2008

2006

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Research Site Phoenix Arizona 85006 —
Research Site Los Angeles California 90095 —
Research Site Sepulveda California 91343 —
Research Site Walnut Creek California 94598 —
Research Site Colorado Springs Colorado 80907 —
Research Site Tamarac Florida 33321 —
Research Site Gainesville Georgia 30501 —
Research Site Auburn Maine 04210 —
Research Site Ann Arbor Michigan 48105 —
Research Site Livonia Michigan 48152 —
Research Site St Louis Missouri 63141 —
Research Site Liverpool New York 13088 —
Research Site Rochester New York 14618 —
Research Site Medford Oregon 97504 —
Research Site Collegeville Pennsylvania 19426 —
Research Site El Paso Texas 79902 —
Research Site San Antonio Texas 78229 —

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 NCT00308191, 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 Mar 7, 2008 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00308191 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →