A randomized controlled trial for validity of aspirin continuation in the preoperative period of intra-peritoneal surgery
Not Applicable
Recruiting
- Conditions
- The patients who need gastroenterological surgery and were treated with prophylactic aspirin due to cardiovascular events
- Registration Number
- JPRN-UMIN000018682
- Lead Sponsor
- Clinical Study Group of Osaka University, Risk Management Group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Not provided
Exclusion Criteria
(1) platelets < 15x10^4/uL (2) active or possible bleeding (3) active infection (4) anti-coagulant use (5) necessary of anti-coagulant for perioperative VTE prophylaxis (6) contraindication of intermittent pneumatic compression for VTE (7) severe complications (e.g. hepatic failure, uncontrollable hypertension, bronchial asthma) (8) allergy for aspirin or heparin (9) history of brain surgery (10) history of MI or angina (11) scheduled other surgery (12) pregnancy (13) mental disorder (14) others
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method