Clinical Outcome of Pericardial Closure Using Gentrix Following Cardiac Surgery

Description

A descriptive comparative project will be conducted to determine if there is a difference in outcomes for adult patients requiring pericardial reconstruction using CorMatrix compared to Gentrix

Conditions

Clinical Outcome of Pericardial Closure Using Gentrix

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Study Overview

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Study Details

Study overview

A descriptive comparative project will be conducted to determine if there is a difference in outcomes for adult patients requiring pericardial reconstruction using CorMatrix compared to Gentrix

Clinical Outcome of Pericardial Closure Using Gentrix Following Cardiac Surgery

Clinical Outcome of Pericardial Closure Using Gentrix Following Cardiac Surgery

Condition
Clinical Outcome of Pericardial Closure Using Gentrix
Intervention / Treatment

-

Contacts and Locations

Dallas

Clinical Research Institute at Methodist Health System, Dallas, Texas, United States, 75203

Dallas

Methodist Dallas Medical Center, Dallas, Texas, United States, 75203

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Must have undergone a Coronary Artery Bypass Grafting(CABG) or valve repair/replacement surgery requiring pericardial reconstruction.

Ages Eligible for Study

18 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Methodist Health System,

Study Record Dates

2024-05-12