Comparative Study on the Post-operative Pain and Other Outcomes of Mesh Fixation With Prolene vs Vicryl vs Skin Staples in Lichtenstein Inguinal Hernia Repair.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorKing Edward Medical University

About this trial

We are going to see the outcome measures for patient and compare them across two groups, those who are undergoing mesh fixation for inguinal hernia by sutures, and those who are fixated by skin staples.

Eligibility criteria

Qualifiers

Patients undergoing inguinal hernia repair

18-65 years

Both genders

Disqualifiers

COPD

Immunocompromised

Obstructive Uropathy

Chronic constipation

Trial design

Treatments tested in this trial

  • Mesh Fixation

Treatment groups

132 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators