A 6 months NIS to evaluate the use of rescue medication and quality of life in adult asthmatic subjects treated with Symbicort® SMART®

Study identifier:NIS-RDE-SYM-2009/1

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A 6 months NIS to evaluate the use of rescue medication and quality of life in adult asthmatic subjects treated with Symbicort® SMART® 1-2 inhalations b.i.d. as maintenance therapy plus additional inhalations as-needed, compared to patients treated with a free combination of an inhaled glucocorticosteroid and an inhaled long acting ß2-agonist plus as needed inhalations of a short acting ß2 agonist.

Medical condition

asthma

Phase

-

Healthy volunteers

No

Study drug

-

Sex

All

Actual Enrollment

500

Study type

Observational

Age

18 Years +

Date

Study Start Date: 01 Apr 2009
Primary Completion Date: -
Study Completion Date: 01 Jun 2010

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Mar 2011 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

CLINRESEARCH GMBH

Inclusion and exclusion criteria