Bioabsorbable Staple Line Reinforcement in Colorectal,Coloanal and Ileoanal Anastomoses



Status:Terminated
Conditions:Colorectal Cancer, Cancer, Colitis, Gastrointestinal, Diverticulitis
Therapuetic Areas:Gastroenterology, Oncology
Healthy:No
Age Range:18 - Any
Updated:4/17/2018
Start Date:April 2008
End Date:October 2012

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Efficacy of Bioabsorbable Staple Line Reinforcement in Colorectal, Coloanal and Ileoanal Anastomoses: A Prospective Randomized Study

The primary purpose of this prospective, randomized multicenter center study is to evaluate
and compare the outcomes of colorectal, coloanal and ileoanal anastomoses reinforced with a
bioabsorbable staple line reinforcement material compared with standard non-reinforced
colorectal, coloanal and ileoanal techniques with respect to the incidence of postoperative
anastomotic leakage, anastomotic stricture and time to ileostomy closure, if applicable.

This is a randomized prospective trial that compares the use of GORE SEAMGUARD® Bioabsorbable
Staple Line Reinforcement (CBSG) to standard stapling techniques in colorectal resections.
The potential exists to utilize CBSG as a means of lowering the rate of post-operative
anastomotic leakage and bleeding in high-risk colorectal, coloanal, and ileoanal anastomoses.

Inclusion Criteria:

- Subjects who will undergo restorative proctectomy or proctocolectomy (<10 cm from anal
verge) with a low circular stapled colorectal, coloanal or ileoanal anastomosis with
or without reservoir, including treatment for rectal cancer, ulcerative colitis,
familial adenomatous polyposis

, diverticulitis, perforation of the bowel/trauma.

- Subjects undergoing Hartmann's reversal with restorative proctectomy (<10 cm from the
anal verge).

- Subjects may or may not have a diverting loop ileostomy as a component of their
initial surgery.

- Subjects who meet the requirements of number 1 and 2, and are being treated for rectal
cancer may or may not have preoperative chemoradiation therapy in the treatment of
their rectal cancer.

Exclusion Criteria:

- Subjects being treated for rectal cancer with a diagnosis of inflammatory bowel
disease.

- Subjects who have significant intraoperative hypotension or cardiac events.

- Subjects with collagen vascular disease, coagulopathy, significant renal or hepatic
dysfunction (creatinine >1.6 or liver enzymes > 50% upper limit of normal values).
We found this trial at
16
sites
307 N University Blvd
Mobile, Alabama 36688
(251) 460-6101
University of South Alabama "University of South Alabama is a public institution that was founded...
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1111 Amsterdam Ave
New York, New York 10025
(212) 523-4000
St Luke's - Roosevelt Hospital Center With 523 beds, Mount Sinai St. Luke's serves as...
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47 New Scotland Ave
Albany, New York 12208
(518) 262-3125
Albany Medical College Albany Medical Center is northeastern New York's only academic health sciences center...
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Barrington, Illinois 60010
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Chicago, Illinois 60612
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Cleveland, OH
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Duluth, Minnesota 55805
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11104 Parkview Plaza Drive
Fort Wayne, Indiana 46845
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Grand Rapids, Michigan 49503
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5255 East Stop 11 Road
Indianapolis, Indiana 46237
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New York, New York 10032
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1001 West Main Street
Peoria, Illinois 61606
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50 North Medical Drive
Salt Lake City, Utah 84132
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8016 Challenger Drive
San Antonio, Texas 78222
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Weston, FL
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