Investigation of the efficacy of Esomeprazole for 8 weeks to the proton pomp inhibitor (PPI)-resistant gastro-esophageal reflux disease (GERD) patients
Not Applicable
- Conditions
- Gastroesophageal
- Registration Number
- JPRN-UMIN000012000
- Lead Sponsor
- ationalOrganizationHospital Fukuyama medical center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1. Severe liver function failure (AST or ALT >100IU/l) 2. Severe heart failure 3. Patients with malignant disease 4. Patients with HIV positive or AIDS 5. Patients received vagolysis 6. Patients received surgery with upper gastrointestinal tract 7. Patients prescribed prohibited concomitant drugs 8. Patients having allergy for Esomeprazole or the similar drugs 9. Patients having difficulty of writing questionnaire sheets 10. Patients who are pregnant 11. Nursing wemen
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method