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NCT Number: NCT07210424

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.

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing inguinal hernia repair
  • 18-65 years
  • Both genders

Exclusion criteria

  • COPD
  • Immunocompromised
  • Obstructive Uropathy
  • Chronic constipation

Treatment and study plan

Mesh Fixation

Procedure

Mesh fixation during Lichtenstein inguinal hernia repair.

Primary outcomes

  1. Post Operative Pain

    Time frame: At 3, 7, 14 and 30 post op day

    Pain scores at 3, 7, 14 and 30 days using a Visual Analogue Pain Scale with values ranging between 0 to 10, 0 meaning no pain and 10 being the highest level of pain.

Sponsors and collaborators

Lead sponsor

King Edward Medical University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Oct 7, 2025
Registry last updated
Dec 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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