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

Stopped early · Not applicable

Conditions studied: Ulcerative Colitis, Familial Polyposis

In brief

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.

Key facts

Study ID

NCT01002287

Run by

Integra LifeSciences Corporation

People needed

11

Starts

2009-10-01

Expected to finish

2011-05-01

Last updated by the study team

2014-11-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of ulcerative colitis or familial polyposis and require two-stage surgery for treatment of either of these disorders will be eligible

Where it is running

• Covidien — Bedford, Massachusetts, United States

Full record on ClinicalTrials.gov

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