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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.

NCT ID: NCT07210424

Last Updated: 2025-12-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

132 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-12-29

Study Completion Date

2026-02-28

Brief Summary

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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.

Detailed Description

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Conditions

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Inguinal Hernia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Skin Staples

Mesh fixation by skin staples

Mesh Fixation

Intervention Type PROCEDURE

Mesh fixation during Lichtenstein inguinal hernia repair.

Sutures

Mesh fixation by sutures (vicryl and prolene)

Mesh Fixation

Intervention Type PROCEDURE

Mesh fixation during Lichtenstein inguinal hernia repair.

Interventions

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Mesh Fixation

Mesh fixation during Lichtenstein inguinal hernia repair.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* COPD
* Immunocompromised
* Obstructive Uropathy
* Chronic constipation
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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King Edward Medical University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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511/RC/KEMU

Identifier Type: -

Identifier Source: org_study_id