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Not yet recruiting NCT06758895

Cardiac Magnetic Resonance Predictors of Outcome of Rhythm Control in Patients with Atrial Fibrillation/Flutter

Observational Rhythm Monitoring

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Rhythm Monitoring. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

evaluate the impact of various features in CMR on the mid-term/long-term success rate of rhythm control for paroxysmal atrial fibrillation/flutter .

Detailed description

* Atrial fibrillation/flutter are widely prevalent. * Reported antiarrhythmic drug efficacy to restore \& maintain sinus rhythm is 52% which is far from optimal. * On the other hand, 5-year arrhythmia-free survival after catheter ablation was previously reported to be 63%. * Therefore, there is a need for better characterization of the underlying atrial substrate, to improve treatment outcomes in terms of efficacy and safety

Primary outcome measures

  • Recurence in patient with AF or flutter after pharmacological or interventional rythm control [Time frame: Baseline]
Secondary outcome measures (1)
  • parameters for safe ablation [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Age>18 years.
  • Patients undergoing successful cardioversion (pharmacologic or electric) for atrial fibrillation/flutter, OR symptomatic patients with paroxysmal atrial fibrillation/flutter scheduled for trans-catheter ablation.
  • Index cardioversion OR Index ablation procedure.

Exclusion criteria

  • LA thrombus on TEE or CMR.
  • Contraindications to CMR.
  • Contraindications to Gd-based contrast.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Assiut Univeristy Heart Hospital — Asyut

Publications

  • 1. Calkins H et al. Circ Arrhythm Electrophysiol. 2009

Identifiers

NCT: NCT06758895 · CMR in rythm control

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗