Study identifier:D961WC00002
ClinicalTrials.gov identifier:NCT03562026
EudraCT identifier:N/A
CTIS identifier:N/A
Specific Clinical Experience Investigation of Nexium in paediatric patients
Peptic Ulcer, Gastroesophageal Reflux
N/A
No
-
All
240
Observational
N/A
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2021 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
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