Trial Search Results

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.

Lead Sponsor:

LifeCell

Stanford Investigator(s):

Intervention(s):

  • Device: Strattice Reconstructive Matrix
  • Other: Standard ostomy creation

Phase:

Phase 4

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