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

J

Jinnah Postgraduate Medical Centre

Status

Enrolling

Conditions

Inguinal Hernia

Treatments

Procedure: Staples for mesh fixation
Procedure: Polypropylene suture for mesh fixation

Study type

Interventional

Funder types

Other

Identifiers

NCT07261189
JPMC-GS-2025-12507

Details and patient eligibility

About

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.

Full description

Inguinal hernia repair is one of the most common general surgical procedures worldwide. The standard method for mesh fixation during Lichtenstein tension-free hernioplasty uses polypropylene sutures. However, skin staples have recently been introduced as a faster and potentially less painful alternative. This randomized controlled trial compares both methods in terms of postoperative pain, measured using the Visual Analogue Scale (VAS), and operative time.

Enrollment

168 estimated patients

Sex

Male

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

168 participants in 2 patient groups

Staples for mesh fixation
Experimental group
Description:
Mesh secured with stainless steel staples during Lichenstein tension-free inguinal hernioplasty
Treatment:
Procedure: Staples for mesh fixation
Polypropylene Suture Group
Active Comparator group
Description:
Mesh secured with polypropylene sutures during Lichensteins tension-free inguinal hernioplasty
Treatment:
Procedure: Polypropylene suture for mesh fixation

Trial contacts and locations

1

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Central trial contact

Asna Ursani, MBBS, FCPS Trainee

Data sourced from clinicaltrials.gov

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