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Completed

NCT Number: NCT02169622

CABG REVEAL: Atrial Fibrillation After Coronary Artery Bypass Graft

Atrial Fibrillation is an abnormal heart rhythm that can occur after coronary heart bypass graft operations. How often this happens and what other problems occur for a person after these operations needs to be better understood. This study uses a device called the Reveal XT, a small device that records heart rhythms to track a patient's heart rhythms after the bypass surgery. The device is implanted at the time the bypass graft is made. The information that is gathered for this study will help physicians to provide better treatment and follow-up of the patients under their care.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Saint Thomas West Hospital

Nashville, Tennessee, 37205, United States

About this study

We will utilize the Reveal XT implantable loop recorder (ILR) in order to monitor the incidence of AF in our post-CABG patients. The Reveal XT has been shown to be superior in comparison to the more commonly used sporadic ECGs.6 Unfortunately, the occurrences of arrhythmias tend to be "unpredictable" and often paroxysmal. Observers are unlikely to have the opportunity to record ECGs at the time of event until it is too late. The ability of the Reveal XT to continuously record ECGs over long periods of time has made it a superior and powerful diagnostic tool in patients with arrhythmias and arrhythmia related complications.

This was evident in the large multicenter PICTURE study whereby a large number of diagnostic tests were undertaken in patients with unexplained syncope without providing conclusive data, but in the same study with the Reveal ILR, the mechanism of syncope in the vast majority of these patients were established often at first onset of an arrhythmia.7

"The equivalent efficacy", if not superiority, of Reveal ILRs above conventional ECGs and Holter-monitors in detecting AF was established in the "XPECT" trial.8 Its sensitivity in detecting events not seen with ECGs and Holter monitoring post COX MAZE procedure (surgical procedure for AF) and post ablations for paroxysmal AF and persistent AF is well established.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 60 years of age or older
  • Presenting for elective Coronary Artery Bypass Graft at Saint Thomas West Hospital

Exclusion criteria

  • Patients <60 years of age
  • Prior cardiac surgery
  • Emergent surgery
  • Need for concomitant cardiac surgery other than PFO closure
  • Prior history of AF or Atrial flutter
  • Prior atrial ablation
  • Prior cardioversion
  • Patients with prior permanent pacemaker
  • Ejection fraction <35%
  • Prior history of thyroid disease
  • Prior history of a cardiomyopathy
  • Patients without telephonic access

Treatment and study plan

Primary outcomes

  1. Number and cost of atrial fibrillation after coronary artery bypass grafting (CABG) per patient

    Time frame: Three year follow-up

    Patient follow up

  2. Number of complication s related to atrial fibrillation in patients after CABG

    Time frame: 3 year follow up

    Patient follow up

  3. Number of therapeutic/intervention changes for participants post CABG resulting from use

    Time frame: 3 year follow up

    Patient follow up

Sponsors and collaborators

Lead sponsor

Saint Thomas Health

Other

Registry information

Official study title

A Prospective Look at Incidence of Atrial Fibrillation After Coronary Artery Bypass Graft and Related Morbidity/Mortality Utilizing the Reveal XT

Important dates

Study start
2013
Primary completion
2017
Study completion
2020
First posted
Jun 23, 2014
Registry last updated
Nov 6, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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