Clinical Trials Logo
  1. Home
  2. Hernia
  3. NCT01205399

A Retrospective Study With Prospective Follow-Up of Complex Ventral Hernia Repair Utilizing the AlloMax Surgical Graft — AlloMax  

Hernia Clinical Trial

Official title:
A Single Arm, Multi-Center, Retrospective Study With Prospective Follow-Up of Complex Ventral Hernia Repair Utilizing the AlloMax Surgical Graft

Clinical Trial Summary

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 AlloMax Surgical Graft at least 9 months in the past will be contacted and asked to take part in this clinical study. The consented subjects' medical records will be reviewed for evidence of any risk factors of hernia recurrence, procedure time, complications and any documented recurrences. The subjects will be asked to undergo a physical exam to rule out any recurrences that were not documented in the medical records.

Clinical Trial Description

Study protocol was amended in June of 2011 to exclude further enrollment of subjects who underwent ventral hernia repair with the AlloMax Surgical Graft to bridge hernia defects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01205399
Study type Observational
Source C. R. Bard
Contact
Status Completed
Phase N/A
Start date September 2010
Completion date October 2011
View Details
See also
  Status Clinical Trial Phase
Completed NCT01629485 - Part vs Whole Task Mastery Training for Laparoscopic Hernia Repair N/A
Terminated NCT01305486 - A Study of Complex Ventral Hernia Repair Utilizing the XenMatrix™ Surgical Graft With Component Separation N/A
Completed NCT01141335 - Polypropylene Mesh Versus Polytetrafluoroethylene (PTFE) Mesh in Inguinal Hernia Repair Phase 4
Completed NCT00905320 - Hernia Repair With or Without Sutures N/A
Completed NCT00535990 - Minimally Invasive Surgery (MIS) Database for the Purpose of Research
Completed NCT00617357 - Repair of Infected or Contaminated Hernias N/A
Withdrawn NCT00138957 - Study of a New Laparoscopic Technique for Parastomal Hernia Repair With Mesh N/A
Completed NCT06034652 - T-GENVIH-003 LTFU (Long Term Follow Up) Study
Completed NCT04119466 - Stabilizing Training in Degenerative Disc Disease N/A
Completed NCT00622583 - International Hernia Mesh Registry
Completed NCT04137172 - Short Term Outcomes of Laparoscopic Intraperitoneal Onlay Mesh With Facial Repair(IPOM-plus) for Ventral Hernia. N/A
Completed NCT01132209 - Suture Techniques to Reduce the Incidence of The inCisional Hernia N/A
Completed NCT00032448 - Does Tension-Free Herniorrhaphy or Laparoscopic Herniorrhaphy Achieve Equal or Better Recurrence Rates and Lower Costs While Achieving Equivalent Outcomes for Hernia Patients? Phase 3
Not yet recruiting NCT05061589 - Incidence and Risk Factors of Parastomal Hernia in Patients With Permanent Colostomy in China
Active, not recruiting NCT02439060 - PUBMIC (Prophylactic Use of Biologic Mesh in Ileal Conduit) N/A
Completed NCT01727388 - Informativeness to Digital Rectal Examination Phase 3
Completed NCT02238964 - Reinforcement of Closure of Stoma Site Phase 2/Phase 3
Completed NCT01997619 - Biological Mesh Repair of Complex Hernias in High Risk Patients N/A
Recruiting NCT00544583 - Continuous Versus Interrupted Abdominal Wall Closure After Emergency Midline Laparotomy Phase 2/Phase 3
Completed NCT03566433 - Postoperative Pain After Endoscopic TEP vs. Lichtenstein Hernioplasty in Inguinal Hernia Repair N/A