Desarda Tissue Technique vs Lichtenstein Technique for Primary Inguinal Hernia Repair

Launched by CONSORCI SANITARI DE L'ALT PENEDÈS I GARRAF · Oct 18, 2024

Keywords

ClinConnect Summary

This clinical trial is looking at two different surgical techniques for fixing a common condition called an inguinal hernia, which occurs when tissue pushes through a weak spot in the abdominal muscles. The trial will compare the Desarda technique, which does not use a mesh, to the Lichtenstein technique, which does use a mesh. Researchers want to find out if one method leads to fewer complications after surgery than the other.

To be eligible for this study, participants must be diagnosed with a primary inguinal hernia and have a body mass index (BMI) below 31. They should also be able to give informed consent and need surgery either as an outpatient or with a planned hospital stay. However, certain patients, such as those with specific health conditions or previous surgeries that may complicate the procedure, will not be included. If you decide to participate, you can expect to undergo one of the two surgical techniques and be monitored for any complications following the surgery.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Diagnosed with primary inguinal hernia.
• • Body mass index below 31
• • Indication for inguinal hernia repair via anterior approach, either as outpatient surgery (CMA) or elective admission.
• • Legal capacity to provide informed consent.
• Exclusion Criteria:
• • Patients with a weak, thin, or divided external oblique aponeurosis.
• * Participants diagnosed with any of the following conditions:
• • Ongoing oncological disease
• • Cirrhotic patients classified as Child B or higher
• • Women who have previously undergone a cesarean section
• • Cognitive or affective conditions that limit the ability to cooperate with the study procedures