Study identifier:D5890L00021
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Physician and patient perception of adjustable maintenance dosing of Symbicort Turbuhaler
perception of physicians & patients of AMD
-
No
Symbicort
All
217
Observational
12 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
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