Study identifier:D9612L00127
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A multicenter, randomized, open-label Phase IV study exploring symptom control rate in co-diagnosed NERD and chronic gastritis patients treated with 8 weeks esomeprazole treatment regimen and 2 weeks esomeprazole treatment regimen
Non Erosive Reflux Disease
Phase 4
No
Esomeprazole
All
305
Interventional
18 Years - 75 Years
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Jun 2015 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Active Comparator: Esomeprazole 8 weeks treatment 20 mg q.d. (quaque die) once a day dosing for 8 weeks | Drug: Esomeprazole 20mg Esomeprazole once daily, 8 weeks and 24 weeks on-demand treatment |
Active Comparator: Esomeprazole 2 Weeks Treatment 20 mg q.d. (quaque die) once a day dosing for 2 weeks | Drug: Esomeprazole 20mg Esomeprazole once daily, 2 weeks and 24 weeks follow up |