A Single Arm, Multi-Center, Retrospective Study With Prospective Follow-Up of Complex Ventral Hernia Repair Utilizing the AlloMax Surgical Graft
| City: |
|
Lexington |
| State: |
|
Kentucky |
| Zip Code: |
|
40536 |
| Conditions: |
|
Hernia |
| Purpose: |
|
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.
|
| Study Summary: |
|
|
| Criteria: |
|
Inclusion Criteria:
- Have undergone a ventral hernia repair using the AlloMax Surgical Graft at least 9
months in the past.
- Have signed an informed consent form (ICF).
Exclusion Criteria:
- Underwent implantation of the AlloMax Surgical Graft for any reason other than
ventral hernia repair.
|
| NCT ID: |
|
NCT01205399 |
| Primary Contact: |
|
Principal Investigator
John S Roth, MD
University of Kentucky
John S Roth, MD
Phone: 859-323-6346 ext. 232
|
| Backup Contact: |
|
N/A |
| Location Contact: |
|
Lexington, Kentucky 40536
United States
There is no listed contact information for this specific location.
Site Status: Recruiting |
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
May 21, 2013 |
| Modifications to this listing: |
|
Only selected fields are shown, please use the link
below to view all information about this clinical trial. |
|
Click to view Full Listing
|