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Completed Phase 3 Interventional Results available

The Fibrin Pad CV Phase III Study

ClinicalTrials.gov ID: NCT02040428

Public ClinicalTrials.gov record NCT02040428. 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 23, 2026, 4:22 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 Single-blinded, Randomized, Controlled, Comparative Phase III Study Evaluating the Safety and Effectiveness of EVARREST™ Fibrin Sealant Patch as an Adjunct to Hemostasis During Cardiovascular Surgery

Study identification

NCT ID
NCT02040428
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ethicon, Inc.
Industry
Enrollment
156 participants

Conditions and interventions

Interventions

  • EVARREST™ Fibrin Sealant Patch Biological
  • Topical hemostat Biological

Biological

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
Dec 31, 2013
Primary completion
Jun 30, 2015
Completion
Aug 31, 2015
Last update posted
Aug 14, 2017

2014 – 2015

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Clinical Investigation Site #15 Atlanta Georgia 30342
Clinical Investigation Site #14 Indianapolis Indiana 46290
Clinical Investigation Site #16 Baltimore Maryland 21201
Clinical Investigation Site #21 Bethesda Maryland 20814
Clinical Investigation Site #17 St Louis Missouri 63110
Clinical Investigation Site #10 Paterson New Jersey 07503
Clinical Investigation Site #12 New York New York 10016
Clinical Investigation Site #20 Philadelphia Pennsylvania 19102
Clinical Investigation Site #18 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02040428, 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 Aug 14, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02040428 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →