Observational Biologic or Prosthetic Mesh
NCT03317665 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 28
Last updated 2021-10-06
Summary
The purpose of this study is to assess the incidence of hernia recurrence with the use of biologic and prosthetic mesh in ventral hernia repair.
Conditions
- Ventral Incisional Hernia
Interventions
- DEVICE
-
Mesh for hernia repair
Permacol, Parietex, Progrip, Strattice Perforated, and Surgimend.
Sponsors & Collaborators
-
Integra LifeSciences Corporation
collaborator INDUSTRY -
University of South Florida
lead OTHER
Principal Investigators
-
Vic Velanovich, MD · University of South Florida
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-02-11
- Primary Completion
- 2021-06-11
- Completion
- 2021-06-11
- FDA Device
- Yes
Countries
- United States
Study Locations
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