This study investigates the treatment of ventral hernias using an investigational bioscaffold. A ventral hernia is a bulge of tissues through an opening of weakness within your abdominal wall muscles. The purpose of this study is to evaluate the early post-operative clinical course and the rate at which hernias return after treatment with the investigational bioscaffold.
Participants in the study will undergo surgery where the investigational bioscaffold is used to reinforce the abdominal wall. The study will track the recovery process and monitor for any recurrence of the hernia after the procedure.
- Who can participate: Participants must be adults aged 18 to 65 years who have been diagnosed with a ventral hernia. Key eligibility factors include not having undergone previous hernia repair with a mesh and not having any active infections or significant comorbidities.
- Study details: Participants will undergo surgery to treat ventral hernias, using an investigational bioscaffold to reinforce the abdominal wall.
