Evaluate onset of effect in patients with Chronic Obstructive Pulmonary Disease (COPD) treated with formoterol Turbuhaler®

Study identifier:D5127C00001

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A randomised, placebo-controlled, double-blind (double-dummy technique),crossover, multi-centre study, to evaluate onset of effect in patients with Chronic Obstructive Pulmonary Disease (COPD) treated with formoterol Turbuhaler® 9 μg, compared with Serevent® Diskus® 50 μg.

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

Phase 2

Healthy volunteers

No

Study drug

Formoterol, Salmeterol, Placebo

Sex

All

Actual Enrollment

109

Study type

Interventional

Age

40 Years +

Date

Study Start Date: 01 Jan 2010
Primary Completion Date: 01 May 2010
Study Completion Date: 01 May 2010

Study design

Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Sept 2012 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria