NCT07210424

Brief Summary

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
132

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 29, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 7, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

December 29, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 29, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2026

Completed
Last Updated

December 17, 2025

Status Verified

December 1, 2025

Enrollment Period

1 month

First QC Date

September 29, 2025

Last Update Submit

December 9, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Post Operative Pain

    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.

    At 3, 7, 14 and 30 post op day

Study Arms (2)

Skin Staples

Mesh fixation by skin staples

Procedure: Mesh Fixation

Sutures

Mesh fixation by sutures (vicryl and prolene)

Procedure: Mesh Fixation

Interventions

Mesh FixationPROCEDURE

Mesh fixation during Lichtenstein inguinal hernia repair.

Skin StaplesSutures

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with inguinal hernia undergoing mesh hernioplasty

You may qualify if:

  • Patients undergoing inguinal hernia repair
  • years
  • Both genders

You may not qualify if:

  • COPD
  • Immunocompromised
  • Obstructive Uropathy
  • Chronic constipation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hernia, Inguinal

Condition Hierarchy (Ancestors)

Hernia, AbdominalHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 29, 2025

First Posted

October 7, 2025

Study Start

December 29, 2025

Primary Completion

January 29, 2026

Study Completion

February 28, 2026

Last Updated

December 17, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share