Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT06159985

Effect of Left Posterior Pericardiotomy for the Prevention of POAF

Led by Seoul National University Hospital · Updated on 2025-05-23

270

Participants Needed

1

Research Sites

159 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is planned to evaluate the effect of left posterior pericardiotomy for the prevention of postoperative atrial fibrillation after coronary artery bypass grafting. Eligible patients will be randomized to be created or not to be created the left posterior pericardiotomy at the end of the operation, and the incidence of postoperative atrial fibrillation will be compared.

CONDITIONS

Official Title

Effect of Left Posterior Pericardiotomy for the Prevention of POAF

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who are planned to undergo coronary artery bypass grafting
  • Patients aged 6519 years
Not Eligible

You will not qualify if you...

  • Patients who are planned to undergo other concomitant cardiac procedures such as valve or aorta procedures
  • Patients who undergo coronary artery bypass grafting using cardiopulmonary bypass
  • Patients documented with paroxysmal, persistent, or permanent atrial fibrillation before operation
  • Patients with a history of cardiac surgery
  • Patients with a history of pericardial disease
  • Patients with severe adhesion at the left pleural cavity preventing effective left posterior pericardiostomy
  • Patients who refuse to participate in this study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Seoul National University Hospital

Seoul, South Korea

Actively Recruiting

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Research Team

H

Ho Young Hwang, MD, PhD

CONTACT

S

Suk Ho Sohn, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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