Study identifier:D9612L00116
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An open label, multicentre study of Nexium (esomeprazole) 40 mg once daily in subjects with symptoms of Gastroesophageal Reflux Disease (GORD) after treatment with a full dose of Proton Pump Inhibitor (PPI)
Gastroesophageal Reflux Disease
Phase 4
No
Esomeprazole 40 mg
All
314
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Aug 2012 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Nexium 40 mgs | Drug: Esomeprazole 40 mg Once a day Other Name: Nexium Procedure/Surgery: Physical Exam every visit Other: Quality of Life Questionnaires every visit Procedure/Surgery: pregnancy test, if applicable as needed |