Chronic Obstructive Pulmonary Disease Clinical Trial
— SYMBOLOfficial title:
Symbicort in Chronic Obstructive Pulmonary Disease
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 |
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 |
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.
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. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
AstraZeneca |
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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