Study identifier:D961HC00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A multicentre, randomised, double-blind, parallel-group, comparative study to compare the efficacy and safety of esomeprazole 20 mg and 40 mg once daily oral administration with omeprazole 20 mg once daily oral administration in patients with reflux esophagitis
reflux esophagitis
Phase 3
No
Esomeprazole, Omeprazole
All
602
Interventional
20 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Dec 2010 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 Esomeprazole 20mg | Drug: Esomeprazole 20mg once daily Other Name: Nexium |
Experimental: 2 Esomeprazole 40mg | Drug: Esomeprazole 40 mg once daily Other Name: Nexium |
Active Comparator: 3 Omeprazole 20mg | Drug: Omeprazole 20mg once daily Other Name: Prilosec |