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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 Oct 18, 2026, 7:04 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 Evaluation of Fibrin Sealant 2 (FS2) as an Adjunct to Hemostasis for Soft Tissue Bleeding During Retroperitoneal or Intra-Abdominal Surgery

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A comparison of fibrin sealant 2 versus Surgicel® as an addition to standard surgical practice in stopping mild to moderate 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

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
Feb 2006 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Jan 9, 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 9, 2009 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00307515 live on ClinicalTrials.gov.

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