A study to evaluate the duration of omeprazole treatment for gastric artificial ulcer after ESD
Not Applicable
Recruiting
- Conditions
- Patients who underwent ESD for the treatment of gastorointestinal stromal tumor (no less than 20 years old)
- Registration Number
- JPRN-UMIN000005750
- Lead Sponsor
- Gifu University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with previous partial gastrectomy or vagotomy 2) Patients receiving anti-coagulants, anti-platelet agents, or steroids 3) Patients with sever cerebral, cardiac, renal, or hematopoietic dysfunction 4) Patients with hypersensitivity to omeprazole 5) Pregnant or lactating women or women who plan to become pregnant during the study 6) Patients who underwent H. pylori eradication after ESD
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method