About this trial
The aims of this study is to compare the efficacy of modified sublay hernioplasty versus intraperitoneal onlay mesh repair for large ventral hernias.
Specifically, this study will assess the primary outcome of recurrence rate one year post surgery and evaluate secondary outcomes, including intraoperative complications, infection rates, pain levels, and post operative hospital stay durations.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age (18-70) years, both sexes.
Fitness for surgery.
Patients with uncomplicated ventral hernia.
Large anterior abdominal wall defect.
Disqualifiers
Patients don't fit for general anesthesia due to sever co-morbidity.
Patients with complicated ventral hernia.
Patient refusal of surgical intervention.
History of bleeding disorders.
Trial design
Parallel
Treatments tested in this trial
Ventral hernia repair
Procedure/SurgeryComparative between both techniques
Treatment groups
Trial outcomes
Primary outcomes
-Recurrence rate one year post operative.
Number of recurrent cases
Secondary outcomes
1-infection rates(number of cases) 2-pain level( according to Visual Analog Score for pain) 3-post operative hospital stay duration(number of days) 4-intra and post operative complications(as iatrogenic injury and adhesions).
The number of cases come with post operative infection , pain(according to pain rating scale) , postoperative days of stay and intraoperative complications.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Ahmed Kahlawy Mahrous Mohamed
Lead sponsor
Assiut University
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: