Pre-operative Withdrawal of Aspirin in Laparoscopic Inguinal Hernia Repair

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

This study aims to assess the need to stop Aspirin before elective laparoscopic inguinal hernia repair. It will consist of 2 arms: patients who continue to take Aspirin perioperatively and patients who stop Aspirin 5-7 days before the surgery. Simple randomization will be performed and allocation is via closed envelope method. The surgeon will be blinded regarding the usage of Aspirin. The primary outcome is the incidence of post-operative hematoma formation within the first 24 hours after surgery. The secondary outcomes are the incidence of post-operative seroma formation within 24 hours, the incidence of post-operative hematoma requiring intervention (including blood transfusion, percutaneous drainage and surgical hemostasis) within 30 days, pain at regular intervals and the incidence of other post-operative complications. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02604732
Study type	Interventional
Source	National University Hospital, Singapore
Contact	Davide Lomanto, MD PhD
Phone	+6567725903
Email	surdl@nus.edu.sg
Status	Recruiting
Phase	N/A
Start date	April 1, 2016
Completion date	May 31, 2024

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