Prospective Trial Comparing the Performance Profiles of Two Non-Cross-Linked Porcine Dermal Matrices in Abdominal Wall Reconstruction

Conditions:   Hernia, Ventral;   Intestinal Fistula;   Fibromatosis, AbdominalInterventions:   Procedure: Abdominal wall reconstruction with Strattice;   Other: Assess pain intensity at last office visit preoperatively;   Other: Assess pain interference at last office visit preoperatively;   Other: Assess physical functioning at last office visit preoperatively;   Other: Assess patient quality of life at last office visit preoperatively;   Other: Assess patient pain intensity postoperatively;   Other: Assess pain interference postoperatively;   Other: Assess physical functioning postoperatively;   Other: Assess quality of life postoperatively;   Other: Assess hernia recurrence at 30 days postoperatively;   Other: Assess bulge at 30 days postoperatively;   Other: Assess Surgical Site Occurrences at 30 days postoperatively;   Other: Assess hernia recurrence at 1 year postoperatively;   Other: Assess bulge at 1 year postoperatively;   Other: Assess Surgical Site Occurrences at 1 year postoperatively;   Other: Assess overall complications at 30 days postoperatively;   Other: Assess overall complications at 1 year postoperatively;   Procedure: Abdominal wall reconstruction with XenMatrix;   Device: Strattice;   Device: XenMatrixSponsor:   Janis, Jeffrey E, MDRecruiting - verified April 2015

Source: ClinicalTrials.gov - August 18, 2014 Category: Research Source Type: clinical trials