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Terminated Not applicable Interventional Results available

Bioabsorbable Staple Line Reinforcement in Colorectal,Coloanal and Ileoanal Anastomoses

ClinicalTrials.gov ID: NCT00663819

Public ClinicalTrials.gov record NCT00663819. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 12:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Study identification

NCT ID
NCT00663819
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
W.L.Gore & Associates
Industry
Enrollment
258 participants

Conditions and interventions

Interventions

  • GORE SEAMGUARD® Bioabsorbable Staple Line Reinforcement Device
  • Staple line without reinforcement Procedure

Device · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2008
Primary completion
Sep 30, 2012
Completion
Sep 30, 2012
Last update posted
Apr 16, 2018

2008 – 2012

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36617
University of Southern California, Keck School of Medicine Los Angeles California 90033
University of South Florida-Cleveland Clinic Florida Weston Florida 33331
Advocate Healthcare/Good Shepard Hospital Barrington Illinois 60010
John Stroger Hospital of Cook County Chicago Illinois 60612
Peoria Surgical Group Peoria Illinois 61606
Colon and Rectal Surgery-NEICRS Group Fort Wayne Indiana 46845
Kenderick Regional Center Indianapolis Indiana 46237
Spectrum Health -Ferguson Group Grand Rapids Michigan 49503
Duluth Clinic Duluth Minnesota 55805
Albany Medical College Albany New York 12208
St. Lukes-Roosevelt Hospital Center New York New York 10019
New York Presbyterian Hospital New York New York 10032
University Hospitals of Cleveland, Case Medical Center Cleveland Ohio 44106-5047
Texas Endosurgery Institute San Antonio Texas 78222
University of Utah Health Sciences Center and Huntsman Cancer Hospital Salt Lake City Utah 84132

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00663819, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 16, 2018 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00663819 live on ClinicalTrials.gov.

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