Symbicort Single Inhaler Therapy vs conventional best practice for the treatment of persistent asthma in adults

Study identifier:D5890L00010

ClinicalTrials.gov identifier:N/A

EudraCT identifier:2005-005974-64

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

A comparison of Symbicort Single Inhaler Therapy (Symbicort Turbuhaler 160/4.5 micrograms, 1 inhalation b.i.d. plus as needed) and conventional best practice for the treatment of persistent asthma in adults - a 26-week, randomised, open-label, parallel-group, multicentre study. Study SPAIN

Medical condition

ASTHMA, BRONCHIAL

Phase

Phase 3

Healthy volunteers

No

Study drug

Symbicort (budesonide/formoterol) Turbuhaler, Conventional treatment

Sex

All

Actual Enrollment

654

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 01 Sept 2006
Primary Completion Date: -
Study Completion Date: 01 Oct 2008

Study design

Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 Nov 2010 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria