Comparing Symbicort® as-Needed or Bricanyl as-Needed or Pulmicort® once daily + Bricanyl as-Needed in asthma patients - MIA

Study identifier:D5890L00032

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A randomised, double blind, placebo controlled, parallel-group study with use of budesonide/formoterol "as-needed", or terbutaline "as-needed" or regular use of budesonide + terbutaline "as-needed", in patients with mild intermittent asthma

Medical condition

Exercise induced asthma

Phase

Phase 2

Healthy volunteers

No

Study drug

budesonide, terbutaline, budesonide/formoterol

Sex

All

Actual Enrollment

66

Study type

Interventional

Age

12 Years +

Date

Study Start Date: 01 Sept 2009
Primary Completion Date: 01 Jul 2010
Study Completion Date: 01 Jul 2010

Study design

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

Verification:

Verified 01 Jul 2012 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria