nonvariceal upper gastrointestinal bleeding
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patient who underwent endoscopy for acute upper gastrointestinal bleeding with proved source of blood losses in upper gastrointestinal tract 2)Patient who was taking antithrombotic medication 3)Patient who was explained about the study, understood it, and gave the consent form
Exclusion criteria
Exclusion criteria: Patient with 1.pregnant or lactating women and women who may be pregnant 2. allrgic to proton pump inhibitor 3.an uncontrollable heart trouble (myocardial infarction, heart failure, or arrhythmia) 4.renal disease, Cre >2mg/dl 5.liver disease, ALT levels that were more than 2.5 times the upper limit of the normal range
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rebleeding rate after resumption of antithrombotic treatment | — |
Countries
Japan
Contacts
shonan kamakura general hospital department of gastroenterology