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Clinical trialNCT01681030CompletedPhase 2Interventional

The Fibrin Pad Cardiovascular Study

SponsorEthicon, Inc.Enrollment42Cardiovascular Disease
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a three-arm, randomized multicenter study evaluating the safety and effectiveness of EVARREST™ Fibrin Sealant Patch in controlling mild to moderate vascular anastomosis suture line bleeding in cardiovascular surgery.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

6 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Clinical Investigation Site #5

    Indianapolis, Indiana, United States

  • Clinical Investigation Site #6

    Kansas City, Missouri, United States

  • Clinical Investigation Site #4

    Camden, New Jersey, United States

  • Clinical Investigation Site #1

    Paterson, New Jersey, United States

  • Clinical Investigation Site #2

    New York, New York, United States

  • Clinical Investigation Site #3

    New York, New York, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

EVARREST™ →Topical hemostat
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 Aug 2012
Primary completion
1 Aug 2013
Completion
3 Sept 2013
Last update posted
12 Jun 2018
Registered enrollment
42
Registry id
NCT01681030

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.