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SYMBICORT® in the Treatment of COPD (SRP COPD)

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ClinicalTrials.gov Identifier: NCT00564499
Recruitment Status : Completed
First Posted : November 28, 2007
Last Update Posted : January 28, 2011
Sponsor:
Information provided by:
AstraZeneca

Brief Summary:
A Scientific Research Program to evaluate the efficacy of SYMBICORT® 320/9μg in the treatment of COPD in real life environment by General Practitioners

Condition or disease
COPD

Study Type : Observational
Observational Model: Case-Crossover
Time Perspective: Prospective
Official Title: A Scientific Research Program to Evaluate the Efficacy of SYMBICORT® 320/9μg in the Treatment of COPD in Real Life Environment by General Practitioners
Study Start Date : March 2006
Actual Study Completion Date : May 2007




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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients
Criteria

Inclusion Criteria:

  • patients (m/f) with COPD (GOLD stadium III and IV)

Exclusion Criteria:

  • patients who recently quit smoking (<3months)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00564499


Sponsors and Collaborators
AstraZeneca
Investigators
Principal Investigator: E Louis, PR Université Libre de Liège

ClinicalTrials.gov Identifier: NCT00564499     History of Changes
Other Study ID Numbers: SRP-RB-COPD-2005/1
First Posted: November 28, 2007    Key Record Dates
Last Update Posted: January 28, 2011
Last Verified: January 2011

Keywords provided by AstraZeneca:
COPD
Symbicort
General Practitioners

Additional relevant MeSH terms:
Budesonide, Formoterol Fumarate Drug Combination
Anti-Asthmatic Agents
Respiratory System Agents