Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT07388108

Atrial Dyssynchrony to Predict Arrhythmias in the Postoperative Setting of Cardiovascular Surgery.

Led by School of Medicine. National University of Cuyo · Updated on 2026-02-10

138

Participants Needed

1

Research Sites

151 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to improve the prediction for developing arrhythmias in the postoperative period of cardiovascular surgery by using non-invasive echocardiographic techniques that are sensitive to detect inter and intra-atrial dyssynchrony. The main question it aims to answer is: Do patients with atrial dyssynchrony are at increased risk of developing arrhythmias in the postoperative period of cardiovascular surgery? Patients admitted to the protocol will undergo an echocardiogram with atrial strain before surgery to determine the presence or absence of intra- and inter-atrial dyssynchrony and will be followed during hospitalization to assess the occurrence of atrial fibrillation in the postoperative period.

CONDITIONS

Official Title

Atrial Dyssynchrony to Predict Arrhythmias in the Postoperative Setting of Cardiovascular Surgery.

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for non-mitral cardiovascular surgery who are in sinus rhythm and have given informed consent
  • No atrial fibrillation present upon hospital admission for surgery
  • Age between 18 and 80 years
Not Eligible

You will not qualify if you...

  • Undergoing mitral or tricuspid valve surgery
  • History of previous atrial fibrillation
  • History of congenital heart disease or cardiac tumors
  • Emergency heart surgery
  • Poor echocardiographic window

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

Clínica de Cuyo

Mendoza, Mendozz, Argentina, 5500

Actively Recruiting

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Research Team

F

Francisco Sánchez, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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