A randomized controlled trial for validity of aspirin continuation in the preoperative period of intra-peritoneal surgery

The requested reference [dad7e44da6af212dea959801e6b64b5cc6980c2f] no longer exists in our database. It has been replaced by the current reference: [4262e9377fe36e531703a7bc975649e1c1359b9b]

Authors
Category Primary study
Registry of TrialsUMIN Clinical Trials Registry
Year 2015
INTERVENTION: aspirin continuation withdraw aspirin (alternative heparin) CONDITION: The patients who need gastroenterological surgery and were treated with prophylactic aspirin due to cardiovascular events PRIMARY OUTCOME: operative blood loss SECONDARY OUTCOME: Adverse events with peri‐operative hemorrhage, transfusion rate, re‐operation rate, hospital stay, cardio‐vasuluar/cardio‐cerebrovascular events, delta hemoglobin INCLUSION CRITERIA: (1) open‐ or laparoscopic‐ cholecystectomy, gastorectomy, or colo‐rectal surgery. (2) more than 3 months aspirin use (3) PS 0‐2 (4) written informed consent
Epistemonikos ID: a9dd27e006741bb46a09c497894ae15f763e36c2
First added on: Aug 23, 2024