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This study will enroll subjects who underwent a ventral hernia repair using the AlloMax Surgical Graft at least 9 months in the past. All subjects who underwent a ventral hernia repair using the Allo...
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Lead Sponsor
C. R. Bard
NCT07608653 · Recurrant Inguinal Hernia
NCT07544238 · Ventral Hernia Midline, Hernia Lumbar, and more
NCT07166172 · Congenital Diaphragmatic Hernia, Congenital Abnormalities, and more
NCT05051254 · Neuromuscular Diseases, Congenital Diaphragmatic Hernia, and more
NCT07476560 · Abdominal Wall Hernia, Umbilical Hernia Repair, and more
University of Kentucky Medical Center
Lexington, Kentucky
Benrus Surgical Associates, Inc
City of Saint Peters, Missouri
Winthrop Surgical Associates, Inc.
Mineola, New York
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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