Duramesh™ versus conventional suture for prevention of trocar-site hernia following laparoscopic surgery (TROCAR): study protocol for a double-blind randomised controlled trial
Lawrence Nip, Sarah Zhao, Rhys Thomas, Paul Bassett, David Ross, Alastair C. J. Windsor, Chris Brew-Graves, Steve Halligan, Samuel G Parker

TL;DR
This study compares a new mesh product, Duramesh, to traditional sutures for preventing hernias after laparoscopic surgery.
Contribution
The trial introduces a novel approach using Duramesh for hernia prevention and aims to provide high-quality evidence.
Findings
The trial will assess hernia incidence at 2 years using ultrasound.
Secondary outcomes include surgical complications and quality of life measures.
Results will provide level 1 evidence for hernia prevention methods.
Abstract
Trocar-site hernia is an underappreciated condition with estimates of approximately 25% at 2 years follow-up. Duramesh™ has emerged as a novel product with potential benefits for incisional hernia prevention. The aim of this trial is to establish if Duramesh is superior to conventional suture for prevention of periumbilical trocar-site hernia following laparoscopic surgery. The TROCAR trial is a prospective single-centre, parallel arm, double-blind randomised controlled trial conducted in the United Kingdom. A total of 250 randomised participants (1:1 ratio) will be allocated to receive either Duramesh or conventional suture (J-vicryl or J-PDS). The primary outcome is the cumulative incidence of sonographically detected periumbilical trocar-site hernia at 2 years of the index operation. Secondary outcomes are 90-day surgical site occurrence (SSO), 90-day surgical site infection (SSI),…
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Taxonomy
TopicsMinimally Invasive Surgical Techniques · Hernia repair and management · Gallbladder and Bile Duct Disorders
