Clinical Prognosis of Patients With Atrial Fibrillation During Radiofrequency Ablation

  • STATUS
    Recruiting
  • End date
    Mar 19, 2024
  • participants needed
    190
  • sponsor
    Centre Hospitalier Universitaire de Nīmes
Updated on 19 August 2021
fibrillation
radiofrequency ablation
cardioversion
persistent atrial fibrillation

Summary

This study is an ancillary study to Isochrone-AF. The investigators hypothesize that patients eligible but non-included in the primary study (patients classified as non-reducible or non-inducible) will have different prognosis and electro-physiclogical characteristics to the patients included and randomized into the Isochrone AF study.

Details
Condition Dysrhythmia, Atrial Fibrillation, Atrial Fibrillation (Pediatric), Arrhythmia
Treatment external electric cardioversion, Wide antrum circle ablation
Clinical Study IdentifierNCT03564327
SponsorCentre Hospitalier Universitaire de Nīmes
Last Modified on19 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

The patient must have given their free and informed consent and signed the consent form
The patient must be a member or beneficiary of a health insurance plan
The patient is at least 18 years old
The patient is available for 18 month follow-up
The patient has paroxysmal or persistent atrial fibrillation

Exclusion Criteria

The subject is participating in a category 1 interventional study, or is in a period of exclusion determined by a previous study
The subject refuses to sign the consent
It is impossible to give the subject informed information
The patient is under safeguard of justice or state guardianship
The patient is pregnant or breastfeeding Early Study Exit Criteria: Patient does not have paroxysmal or persistent AF at the time of inclusion
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