A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using Parietex™ Composite Ventral Patch
NCT01848184 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 126
Last updated 2018-07-20
Summary
The objective of this study is to assess the recurrence rate following the use of PARIETEX™ Composite Ventral Patch in primary ventral hernia repair by open approach with intra-peritoneal positioning.
Conditions
- Hernia
Interventions
- DEVICE
-
PARIETEX™ Composite Ventral Patch
PARIETEX™ Composite Ventral Patch for ventral hernia repair
Sponsors & Collaborators
-
Medtronic - MITG
lead INDUSTRY
Principal Investigators
-
Frederik Berrevoet, MD · University Hospital Ghent (Belgium)
-
Lars N Jørgensen, MD · Bispebjerg Hospital, University of Copenhagen (Denmark)
-
Carl Doerhoff, MD · Surgicare of MO (United States)
-
Steven Hopson, MD · Hernia Centers of Excellence, VA (United States)
-
Eric KULLMAN, MD · Medicinskt Centrum i Linköping (Sweden)
-
Marco G MUZI, MD · Department of Surgery, University Hospital Tor Vergata, Roma (Italy)
-
Simon NIENHUIJS, MD · Catharina Ziekenhuis, EJ EINDHOVEN (The Netherlands)
-
Filip E Muysoms, MD · Algemene Heelkunde, AZ Maria Middelares Ghent (Belgium)
-
Tim Tollens, MD · Imelda Hospital, Bonheiden (Belgium)
-
Karl Leblanc, MD · Our Lady of the Lake Regional Medical Center, LA (United States)
-
Mark Schwartz, MD · Monmouth Medical Center, NJ (United States)
-
Vic Velanovich, MD · University of South Florida (United States)
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-05-31
- Primary Completion
- 2016-07-31
- Completion
- 2016-07-31
Countries
- United States
- Belgium
- Denmark
- Sweden
Study Locations
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