Is a
Clinical Study attributes
NCT Number
Trial Recruitment Size
1720
Trial Sponsor
Clinical Trial Start Date
2008
0Primary Completion Date
2012
0Study Completion Date
2012
0Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Device0
Intervention Name
Inguinal hernia repair with Strattice0
Inguinal hernia repair with Ultrapro0
Interventional Trial Phase
Phase 40
Participating Facility
Official Name
Prospective, Randomized, Controlled, Third-Party Blinded Multicenter Evaluation of Strattice/LTM in the Repair of Inguinal Hernias0
Last Updated
May 10, 2016
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Double0
Masked Party
Participant0
Outcomes Assessor0
Study summary
This is a prospective, randomized, controlled, third-party blinded, multicenter, interventional evaluation of inguinal hernia repair comparing Strattice to light weight polypropylene mesh. Performance and outcomes measures to be compared include postoperative resumption of activities of daily living, nature and incidence of short- and long-term pain and complications, and incidence of hernia recurrence.
Timeline
No Timeline data yet.
Further Resources
No Further Resources data yet.
