A Prospective Study of Fortiva in Hernia Repair
NCT06101979 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 120
Last updated 2025-07-25
Summary
The goal of this study is to evaluate safety and performance of the Fortiva Tissue Matrix. Participants will complete questionnaires to measure outcomes after hernia surgery for two years.
Conditions
- Ventral Hernia
- Incisional Hernia
- Abdominal Wall Reconstruction
Interventions
- DEVICE
-
Fortiva Tissue Matrix
Acellular Dermal Matrix used in hernia surgery
Sponsors & Collaborators
-
RTI Surgical
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-11-15
- Primary Completion
- 2027-12-31
- Completion
- 2027-12-31
Countries
- United Kingdom
Study Locations
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