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Completed Not applicable Interventional Results available

Evaluation Of New Onset Postoperative Atrial Fibrillation

ClinicalTrials.gov ID: NCT01247974

Public ClinicalTrials.gov record NCT01247974. 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 26, 2026, 8:11 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

Prospective, Randomized Evaluation of New Onset Postoperative Atrial Fibrillation in Subjects Receiving the CorMatrix® ECM® for Pericardial Closure

Brief summary

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

This is a multi-center, prospective, randomized and controlled clinical trial comparing the safety and efficacy of the CorMatrix ECM for Pericardial Closure to reduce the incidence of new onset postoperative atrial fibrillation by circumferentially reconstructing the normal pericardial anatomy following isolated, first-time, CABG procedures compared to subjects that do not undergo pericardial closure. This trial will be conducted at up to 20 clinical sites in the U.S.

Study identification

NCT ID
NCT01247974
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Elutia Inc.
Industry
Enrollment
439 participants

Conditions and interventions

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 2010 (Type not available)
Primary completion
Dec 2012 (Actual)
Completion
Dec 2012 (Actual)
Last update posted
Jul 27, 2023

2010 – 2012

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Trinity Medical Center Birmingham Alabama 35213 —
Southeast Alabama Medical Center Dothan Alabama 36301 —
Mobile Infirmary Medical Center Mobile Alabama 36607 —
Providence Hospital Mobile Alabama 36608 —
Saint Agnes Medical Center Fresno California 93720 —
Stanford University School of Medicine Stanford California 94305 —
St. Vincent's Hospital Jacksonville Florida 32204 —
Florida Hospital Orlando Florida 32803 —
Advocate Christ Medical Center Oak Lawn Illinois 60453 —
Saint Francis Heart Center Indianapolis Indiana 46237 —
St. Luke's Hospital Kansas City Missouri 64111 —
Columbia University Medical Center New York New York 10032 —
The Ohio State University Medical Center Columbus Ohio 43210 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Baptist Memorial Hospital Memphis Tennessee 38120 —
Swedish Medical Center Seattle Washington 98122 —

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 NCT01247974, 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 Jul 27, 2023 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01247974 live on ClinicalTrials.gov.

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