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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00611520
Other study ID # 1312005009
Secondary ID
Status Completed
Phase N/A
First received January 29, 2008
Last updated January 27, 2011
Start date September 2005

Study information

Verified date January 2011
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

Under daily routine conditions and without any intervention by the sponsor regarding the selection of subjects, diagnostic procedures, therapeutic decisions (medicinal and non- medicinal therapy, dose, duration, etc.), routine assessments, the participating physicians (i.e. pneumologists and internists) are asked to document relevant data related to the budesonide/formoterole therapy in patients with COPD.


Recruitment information / eligibility

Status Completed
Enrollment 64730
Est. completion date
Est. primary completion date December 2005
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with COPD treated with budesonide/formoterol

Exclusion Criteria:

- limitations; possible risks; warnings; contraindications mentioned in the SPC.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Outcome

Type Measure Description Time frame Safety issue
Secondary to get further insight into the details of the use , dosage scheme and duration of treatment with budesonide /formoterol in this population
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