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Completed Phase 3 Interventional

Evaluation of Fibrin Sealant 2 in Retroperitoneal or Intra-Abdominal Surgery

ClinicalTrials.gov ID: NCT00307515

Public ClinicalTrials.gov record NCT00307515. 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 May 19, 2026, 7:07 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

A Prospective, Randomized, Controlled Evaluation of Fibrin Sealant 2 (FS2) as an Adjunct to Hemostasis for Soft Tissue Bleeding During Retroperitoneal or Intra-Abdominal Surgery

Study identification

NCT ID
NCT00307515
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ethicon, Inc.
Industry
Enrollment
135 participants

Conditions and interventions

Interventions

  • Fibrin Sealant 2 (FS2) Drug
  • Oxidized Regenerated Cellulose (Surgicel) Device

Drug · Device

Eligibility (public fields only)

Age range
Not listed
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
Jan 31, 2006
Primary completion
Nov 30, 2006
Completion
Nov 30, 2006
Last update posted
Jan 8, 2009

2006

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Children's Hospital of Los Angeles Los Angeles California 90027
Jacksonville Center for Clinical Research Jacksonville Florida 32216
Miami Research Associates Miami Florida 33173
Medical College of Georgia Augusta Georgia 30912
The Iowa Clinic Des Moines Iowa 50309
St. Agnes Healthcare, Inc. Baltimore Maryland 21229
Massachusetts General Hospital Boston Massachusetts 02114
Cooper University Hospital Camden New Jersey 08103
Mt. Sinai Hospital New York New York 10029
GYN Oncology Associates Syracuse New York 13202
Oregon Health and Science University Portland Oregon 97239
Lehigh Valley Hospital Allentown Pennsylvania 18103
Children's Hospital of Pittsburgh Pittsburgh Pennsylvania 15206
Lankenau Hospital Wynnewood Pennsylvania 19096
MD Anderson Cancer Center Houston Texas 77030
The 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 NCT00307515, 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 Jan 8, 2009 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00307515 live on ClinicalTrials.gov.

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