Is a
Clinical Study attributes
NCT Number
Trial Recruitment Size
1200
Trial Sponsor
Clinical Trial Start Date
2008
0Primary Completion Date
2012
0Study Completion Date
2012
0Clinical Trial Study Type
Interventional0
Intervention Type
Other0
Device0
Intervention Name
Standard ostomy creation0
Strattice Reconstructive Matrix0
Interventional Trial Phase
Phase 40
Participating Facility
Official Name
A Prospective, Multicenter, Randomized, Controlled, Third-party Blinded Study of Strattice Fascial Inlay for Parastomal Reinforcement in Patients Undergoing Surgery for Permanent Abdominal Wall Ostomies0
Last Updated
September 28, 2015
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Participant0
Care Provider0
Outcomes Assessor0
Study summary
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.
Timeline
No Timeline data yet.
Further Resources
No Further Resources data yet.
