NCT01002287

An Evaluation of SprayShield in Reducing Post-Operative Adhesion Formation Following Major Open Abdominal Surgery

An Evaluation of the SprayShield Adhesion Barrier System in Reducing Post-Operative Adhesion in Abdominal Surgery

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 11 (actual)
• Sponsor: Integra LifeSciences Corporation · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This will be a prospective, multi-center, randomized, single blind study to collect and evaluate post-market clinical data on the SprayShield Adhesion Barrier System as an adjuvant to good surgical technique for the reduction of postoperative adhesion formation following major open abdominal surgery.

Conditions

• Ulcerative Colitis
• Familial Polyposis

Interventions

Type	Name	Description
DEVICE	SprayShield Adhesion Barrier System	Adhesion Barrier Device
PROCEDURE	Good Surgical Technique Alone	Good Surgical Technique Alone

Timeline

• Start date: 2009-10-01
• Primary completion: 2010-10-01
• Completion: 2011-05-01
• First posted: 2009-10-27
• Last updated: 2014-11-20
• Results posted: 2014-01-29

Locations

1 site across 1 country: United States