Clinical Prognosis of Patients With Atrial Fibrillation During Radiofrequency Ablation (Isochrone-AFAn)

Centre Hospitalier Universitaire de Nīmes

Status: Completed

Conditions: Atrial Fibrillation

Treatments: Procedure: External electric cardioversion

Study type: Interventional

Funder types: Other

Identifiers

NCT03564327

NIMAO/2017-03/MG-02

Details and patient eligibility

About

Identify the parameters of the predictive isochronous map for the clinical outcome of radiofrequency ablation in terms of absence of documented atrial fibrillation recurrence at 18 months.

Enrollment: 175 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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175 participants in 1 patient group

patients with atrial fibrillation

Experimental group

Treatment:

Procedure: External electric cardioversion