Looking for volunteers
Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh
NCT04779918 · Tela Bio Inc · Updated 5 May 2026
- What is being tested
- OviTex Reinforced Tissue Matrix
- For
- Hernia, Ventral; Hernia, Inguinal
- Kind of study
- Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
- Who can join
- Ages 21 years and older. About 160 people. The full rules are on the registry page.
- Where
- United States (10 sites)
- When
- Starts or started 29 April 2021, ends 30 Dec 2029. Registered 3 March 2021.
- Results
- None posted yet.
In the researchers' words
This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.
Sites
- University of South AlabamaMobile, Alabama, United States
- SurgOneDenver, Colorado, United States
- GenesisCareDestin, Florida, United States
- Surgical Healing Arts CenterFort Myers, Florida, United States
- St. Luke's HospitalOverland Park, Kansas, United States
- University of LouisvilleLouisville, Kentucky, United States
- Munson HealthcareTraverse City, Michigan, United States
- St. Francis HospitalRoslyn, New York, United States
- Mohawk Valley Health SystemUtica, New York, United States
- Houston MethodistHouston, Texas, United States