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Clinical Trial Summary

A comparison of ventral hernia repair with Strattice and Fortiva mesh.Primary The study team aims to determine the hernia recurrence rates for RTI Surgical biologic mesh (Fortiva) compared to Strattice. Also the study team aims to determine the mesh related complications for RTI Surgical biologic mesh (Fortiva) compared to Strattice


Clinical Trial Description

This study will be a prospective, matched study of patients using Fortiva biologic mesh to determine the rates of hernia recurrence and mesh related complication compared to Strattice mesh. Patients who meet the inclusion and exclusion criteria will be prospectively enrolled to receive a Ventral Hernia Repair (VHR) using Fortiva biologic mesh and will be compared to a retrospective cohort of patients with a VHR that utilized Strattice mesh. Patients will be propensity matched in a 1:3 (Fortiva : Strattice) fashion based on age, sex, and hernia defect size. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05572021
Study type Interventional
Source Wake Forest University Health Sciences
Contact Gregory T Scarola, MS
Phone 704-355-5379
Email Gregory.Scarola@Atriumhealth.org
Status Recruiting
Phase N/A
Start date September 25, 2023
Completion date February 2025

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