This study is currently not recruiting participants.

Short Term Outcomes for Hybrid Mesh Use (Ovietex vs. Zenapro vs. Synecor)

Investigating Mesh Types in Ventral Hernia Repair

Not Recruiting
100 years or below
All
Phase N/A

Brief description of study.

The purpose of this study is to determine if the use of biosynthetic (hybrid) mesh in contaminated ventral hernia repair will lead to lower rates of infection and hernia recurrence as compared to biologic or synthetic meshes alone.

Detailed description of study

The purpose of this study is to determine if the use of biosynthetic (hybrid) mesh in contaminated ventral hernia repair will lead to lower rates of infection and hernia recurrence as compared to biologic or synthetic meshes alone.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: ventral hernia
  • Age: 100 years or below
  • Gender: All

This study investigates the use of different types of mesh in repairing ventral hernias, which are openings or bulges in the abdominal wall. The purpose is to see if using a biosynthetic (hybrid) mesh reduces the chances of infection and hernia coming back compared to using just biologic or synthetic meshes.

Participants in this study will undergo a surgical procedure to repair a ventral hernia. The study will compare outcomes between those receiving the biosynthetic mesh and those receiving either biologic or synthetic mesh. The study aims to find out which type of mesh is more effective in reducing complications.

  • Who can participate: To participate, individuals must meet specific age criteria and other eligibility factors, which may include the size and location of the hernia and overall health status.
  • Study details: Participants will be assigned to receive either the biosynthetic mesh or one of the other mesh types during their hernia repair surgery.
Updated on 19 Feb 2024. Study ID: 1801998827

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