JPRN-UMIN000006344
Not yet recruiting
Phase 4
Evaluation of abdominal symptoms and gastrointestinal mucosal injuries in patients receiving oral anticoagulant dabigatran - Evaluation of abdominal symptoms and gastrointestinal mucosal injuries in patients receiving oral anticoagulant dabigatran
Conditionspper gastrointestinal mucosal injury
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- pper gastrointestinal mucosal injury
- Sponsor
- Kobe University Hospital
- Enrollment
- 50
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •a. Patients with severe renal failure including those on hemodialysis (creatinine clearance of less than 30mL/min) b. Patients having organic lesions with a risk of bleeding (within 6 months after the onset of hemorrhagic stroke) c. Patients with a spinal/epidural catheter inserted or those in which the spinal/epidural catheter was just removed within 1 hour d. Patients with a history of hypersensitivity for tabeprazole, famotidine, or rebamipide e. Patients who are taking itraconazole f. Patients judged by investigators as ineligible for study enrollment
Outcomes
Primary Outcomes
Not specified
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