CompletedNot Applicable

MEsh FIxation in Laparoendoscopic Repair of Large M3 Inguinal Hernias

Poland204 participantsStarted 2023-02-01

Plain-language summary

The goal of this Multicenter Clinical Trial is to verify the hypothesis that non-fixation of the 3-D anatomical mesh (Dextile Anatomical Mesh or 3D Max Mesh) is non-inferior in terms of recurrence compared to fixation of lightweight, macroporous meshes in laparoendoscopic repairs of large M3 inguinal hernias.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * elective groin hernia repair, * M3 or M3+L1-3 (EHS classification) groin hernia confirmed during surgery * eligibility to laparoendoscopic repair * written informed consent Exclusion Criteria: * emergency surgery (incarcerated hernia) * contaminated surgical field * recurrent hernia * extremely large scrotal hernia with the need of other forms of prevention of Abdominal Compartment Syndrome (botox injection, preoperative progressive pneumoperitoneum - PPP, bowel resection etc.)

What they're measuring

Reccurence Rate

Timeframe: 12-months

Trial details

NCT IDNCT05678465

SponsorSwissmed Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-11-30

View on ClinicalTrials.gov More Hernia, Inguinal trials