Comparative Analysis of Onlay and Sublay Mesh Repair Techniques in Umbilical Hernia Surgery
This study aims to compare the effectiveness of two surgical techniques, onlay and sublay mesh repair, in the treatment of umbilical hernias.
Onlay Mesh Repair
+ Sublay Mesh Repair
Treatment Study
Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.Umbilical hernia repair is a common surgical procedure, with the use of prosthetic mesh proven to reduce recurrence rates compared to traditional stitch repair. Two popular mesh techniques are onlay and sublay repairs, each with unique advantages and disadvantages. Onlay repair involves placing the mesh over the hernia, while sublay repair positions the mesh underneath. This study aims to compare these two techniques in adult patients undergoing umbilical hernia surgery, with the goal of improving care and providing evidence-based decisions in clinical practice. Patients participating in this study will undergo either onlay or sublay mesh repair for their umbilical hernia. The study will record details such as demographic characteristics, hernia features, and operative specifics. Primary outcome measures include postoperative complication rates and hernia recurrence, while secondary measures include operative time, length of hospital stay, and early postoperative morbidity. Patients will be followed postoperatively according to standard clinical practice to assess surgical outcomes. The results are expected to provide valuable comparative data on the safety and effectiveness of both techniques.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.116 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 90 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Bakırköy Dr. Sadi Konuk Training and Research Hospital
Istanbul, Turkey (Türkiye)Open Bakırköy Dr. Sadi Konuk Training and Research Hospital in Google Maps