A multicentre, randomised, double-blind, double dummy, parallel group study to compare the salmeterol/fluticasone propionate combination SERETIDE at a dose of 50/100mcg twice daily and fluticasone propionate FLIXOTIDE at a dose of 200mcg twice daily, both delivered via a dry powder inhaler DISKUS for 12 weeks in asthma in children aged 4-11 years not controlled by inhaled corticosteroids alone at medium dose
- Conditions
- Asthma in children aged 4-11 years not controlled by inhaled corticosteroids alone at medium dose.MedDRA version: 6.1Level: PTClassification code 10003553
- Registration Number
- EUCTR2005-002949-40-IT
- Lead Sponsor
- GLAXO SMITHKLINE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 506
Inclusion Criteria
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method