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NCT03564327Completed

Clinical Prognosis of Patients With Atrial Fibrillation During Radiofrequency Ablation

Clinical Prognosis of Patients With Atrial Fibrillation During Radiofrequency Ablation and Interest of the Isochron Map

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
175 (actual)
First submitted
11 Jun 2018
Start date
14 Feb 2019
Primary completion date
9 Feb 2023
Lead sponsor
Centre Hospitalier Universitaire de Nīmes
NCT number
NCT03564327

What you commit to

  • Study type: Interventional
  • Participants enrolled: 175
  • From 14 Feb 2019 to the primary completion date, 9 Feb 2023
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The subject is participating in a category 1 interventional study, or is in a period of exclusion determined by a previous study

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHU Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
CHU Nîmes
Coordinator of this site? Confirm its status
NîmesFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.