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Completed Phase 2 Interventional Results available

The Fibrin Patch Soft Tissue Study

ClinicalTrials.gov ID: NCT00658723

Public ClinicalTrials.gov record NCT00658723. 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, 2:00 AM EDT

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

Official title

A Prospective, Randomized, Controlled, Superiority Evaluation of Fibrin Patch as an Adjunct to Control Soft Tissue Bleeding During Abdominal, Retroperitoneal, Pelvic, and Thoracic Surgery

Study identification

NCT ID
NCT00658723
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ethicon, Inc.
Industry
Enrollment
141 participants

Conditions and interventions

Conditions

Interventions

  • Fibrin Pad Drug
  • SURGICEL™ Device

Drug · Device

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
Feb 29, 2008
Primary completion
Mar 31, 2009
Completion
Apr 30, 2009
Last update posted
Sep 10, 2014

2008 – 2009

United States locations

U.S. sites
11
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294
Jacksonville Center for Clinical Research Jacksonville Florida 32216
Baptist Hosptial Miami Florida 33173
Emory University Hospital Atlanta Georgia 30322
Medical College of Georgia Augusta Georgia 30912
University of Maryland Medical Center Baltimore Maryland 21201
St. Agnes Healthcare, Inc. Baltimore Maryland 21229
Long Island Jewish Medical Center New Hyde Park New York 11040
Lehigh Valley Hospital Allentown Pennsylvania 18103
The University of Texas MD Anderson Cancer Center Houston Texas 77030
Weill Medical Colleges of Cornell University - Methodist Hospital Houston Texas 77030

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 NCT00658723, 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 Sep 10, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00658723 live on ClinicalTrials.gov.

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