Actively Recruiting

Age: 18Years +
All Genders
NCT06523738

Left Atrial Volume Changes Who Underwent Cardioversion and Recurrence of AF After RF Ablation in Persistent AF (SAFE-AF)

Led by The Second Affiliated Hospital of Chongqing Medical University · Updated on 2024-07-26

100

Participants Needed

1

Research Sites

339 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Electrical/pharmacological cardioversion improves structural remodeling of left atrium. We hypothesize that persistent atrial fibrillation (AF) patients with more significant left atrial size reduction after cardioversion have lower AF recurrence rates following radiofrequency ablation. The aim is to evaluate the relationship between changes in left atrial size 3 to 6 months after cardioversion and the recurrence rate of atrial fibrillation following radiofrequency ablation.

CONDITIONS

Official Title

Left Atrial Volume Changes Who Underwent Cardioversion and Recurrence of AF After RF Ablation in Persistent AF (SAFE-AF)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with persistent atrial fibrillation within the past 6 months
  • Left atrial diameter between 40 mm and 50 mm before study
  • Successful pharmacological or electrical cardioversion performed
  • At least two echocardiograms before and 3-6 months after cardioversion confirming left atrial size status
  • Provided informed consent to participate
Not Eligible

You will not qualify if you...

  • Previous radiofrequency ablation treatment for atrial fibrillation
  • Past cardiac surgery
  • Cognitive impairments preventing informed consent

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Second Affiliated Hospital of Chongqing Medical University

Chongqing, Chongqing Municipality, China, 400072

Actively Recruiting

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Research Team

Y

Yuehui Yin, MD

CONTACT

F

Fang Qin, MD

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

2

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