This study is looking at how well OviTex Reinforced Tissue Matrix works when used to repair ventral or inguinal hernias (a bulge caused by an organ pushing through a weak spot in muscle or tissue) using robotic surgery. All participants will receive OviTex during their hernia repair. Researchers will be watching for any surgical site issues or complications that happen within the first three months after surgery. You may be able to join if you are at least 21 years old, have a ventral or inguinal hernia needing surgical repair, and are scheduled for a robotic repair using OviTex. The study aims to enroll up to 160 people. The current recruitment status is unclear.

Study design

This is a single-arm study, meaning all 160 participants will receive the OviTex device. There is no specified phase for this interventional study.

What's involved

Not specified in the trial record.

Compensation

Not stated in the trial record.

Follow-up

Participants will be followed for early surgical site occurrences and post-operative complications within the first three months after surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.