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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00772733
Other study ID # NIS-RDK-DUM-2007/1
Secondary ID
Status Completed
Phase N/A
First received October 14, 2008
Last updated February 21, 2011
Start date October 2008
Est. completion date December 2010

Study information

Verified date February 2011
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

The purpose of this study is to ensure the quality of the COPD treatment in primary care by implementing planned follow-up visits, where the disease condition is evaluated and optimised in accordance with the national COPD recommendations. If relevant the general practitioner (GP) will refer patients to COPD rehabilitation conducted by relevant municipality rehabilitation teams. Secondarily the purpose is to improve collaboration and communication between the local hospital pulmonologist, GPs and the municipality rehabilitation team


Recruitment information / eligibility

Status Completed
Enrollment 936
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 35 Years and older
Eligibility Inclusion Criteria:

- COPD diagnose, verified by spirometry

- Having given informed consent

Exclusion Criteria:

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Research Site Aalborg
Denmark Research Site Arhus
Denmark Research Site Bjerringbro Viborg
Denmark Research Site Klarup
Denmark Research Site Moldrup Viborg
Denmark Research Site Orum
Denmark Research Site Skals Viborg
Denmark Research Site Skive
Denmark Research Site Spottrup
Denmark Research Site Stoholm
Denmark Research Site Viborg

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Control visits at General practitioners 6-12 months No
Primary Lung function measured by spirometry 6-12 months No
Secondary Dyspnoea on MRC scale 6-12 months No
Secondary Smoking status 6-12 months No
Secondary Rehabilitation completed in the municipality rehabilitation team 6-12 months No
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