Clinical Outcome of Pericardial Closure Using Gentrix Following Cardiac Surgery

Stopped early

Conditions studied: Clinical Outcome of Pericardial Closure Using Gentrix

In brief

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

Key facts

Study ID

NCT06136182

Run by

Methodist Health System

People needed

489

Starts

2023-05-12

Expected to finish

2026-04-08

Last updated by the study team

2026-05-01

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Must have undergone a Coronary Artery Bypass Grafting(CABG) or valve repair/replacement surgery requiring pericardial reconstruction.
• CABG or valve repair/replacement surgery must have been either elective or urgent status

You may not qualify if…

• CABG or valve repair/replacement surgery classified as emergent status Surgery classified as redo-sternotomy

Where it is running

• Clinical Research Institute at Methodist Health System — Dallas, Texas, United States
• Methodist Dallas Medical Center — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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