Education and Training
Parastomal Reinforcement With Strattice
The purpose of this study is to compare the clinical outcomes of patients undergoing surgery for a permanent abdominal wall ostomy with and without placement of Strattice fascial inlay, as measured by postoperative occurence of parastomal hernia.
Stanford is currently not accepting patients for this trial.
Stanford Investigator(s):
Intervention(s):
- other: Standard ostomy creation
- device: Strattice Reconstructive Matrix
Eligibility
Inclusion Criteria:
- adults
- need for permanent ileostomy or colostomy
Exclusion Criteria:
- history of hernia at new ostomy site
- has previously implanted surgical mesh at site of planned ostomy
- requires a temporary ostomy
- has need for multiple ostomies
- is receiving chronic immunosuppression therapy, has MELD score of > 17, has severe
COPD, systemic infection, or known collagen disorder
- is bedridden or otherwise non-ambulatory
Ages Eligible for Study
18 Years - N/A
Genders Eligible for Study
All
Not currently accepting new patients for this trial
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Moe Jalali
6507244023
Not Recruiting