Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05599750

Suture Repair vs Mesh Repair for Incisional Hernia

A Modern Comparison of Suture Repair With Mesh Repair for Incisional Hernia

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
154 (estimated)
Sponsor
Clayton Petro · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this randomized controlled trial is to compare the difference in quality of life at one year postoperatively for patients undergoing incisional hernia repair with mesh versus suture repair using modern techniques. The main question it aims to answer are: • Determine if primary suture repair is non-inferior to mesh repair for incisional hernias 2-6cm with respect to quality of life using the HerQLes summary score at one year postoperatively.

Detailed description

This is a patient-blinded randomized control trial comparing incisional hernia repair using synthetic mesh versus suture repair. This is a non-inferiority trial theorizing that suture repair will be non-inferior with respect to quality of life (using the HerQLes survey) at 1 year postoperatively. Patients will be blinded to the intervention, groups will be in parallel.

Conditions

Interventions

TypeNameDescription
PROCEDUREIncisional hernia repairParticipants will undergo incisional hernia repair

Timeline

Start date
2022-11-14
Primary completion
2026-10-01
Completion
2031-10-01
First posted
2022-10-31
Last updated
2026-01-07

Locations

5 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT05599750. Inclusion in this directory is not an endorsement.