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Recruiting NCT07261189

Comparing Staples Versus Polypropylene Sutures for Mesh Fixation in Inguinal Hernia Repair in Terms of Postoperative Pain

Trial Parameters

Condition Inguinal Hernia
Sponsor Jinnah Postgraduate Medical Centre
Study Type INTERVENTIONAL
Phase N/A
Enrollment 168
Sex MALE
Min Age 20 Years
Max Age 60 Years
Start Date 2025-09-01
Completion 2026-03
Interventions
Staples for mesh fixationPolypropylene suture for mesh fixation

Brief Summary

This randomized controlled trial aims to compare postoperative pain between staples and polypropylene sutures used for mesh fixation in patients undergoing elective Lichtenstein tension-free inguinal hernia repair.

Eligibility Criteria

Inclusion Criteria: * Male patients aged 20 to 60 years. * Patients undergoing elective Lichtenstein tension-free mesh repair for unilateral, uncomplicated inguinal hernia (direct or indirect). * Body Mass Index (BMI) between 19 and 30 kg/m². * ASA physical status I, II, or III. * Patients willing to participate and provide informed consent. Exclusion Criteria: * Diabetic patients (on medical records). * Bilateral or recurrent inguinal hernia. * Complicated hernia (irreducible, obstructed, or strangulated). * Patients unwilling to participate or who fail to complete follow-up.

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