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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
NCT07544238 · Ventral Hernia Midline, Hernia Lumbar, and more
NCT07166172 · Congenital Diaphragmatic Hernia, Congenital Abnormalities, and more
NCT07476560 · Abdominal Wall Hernia, Umbilical Hernia Repair, and more
NCT07473583 · Hernia, Inguinal, Inguinal Hernia
NCT07319156 · Cervical Radiculopathy, Proprioception, 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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