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Clinical Trials/NCT03332862
NCT03332862
Unknown
Not Applicable

Acute Efficacy of Point-by-point Radiofrequency Ablation for Pulmonary Vein Isolation in Patients With Atrial Fibrillation: a Randomized Comparison of Continuous Versus Discontinuous Design of Encircling Lesions

Institute for Clinical and Experimental Medicine1 site in 1 country30 target enrollmentSeptember 15, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
Institute for Clinical and Experimental Medicine
Enrollment
30
Locations
1
Primary Endpoint
Combined unsuccessful PVI or PV reconnection
Last Updated
8 years ago

Overview

Brief Summary

Acute efficacy of point-by-point radiofrequency ablation for pulmonary vein isolation in patients with atrial fibrillation are comparable independantly of the ablation strategy (continous versus discontinuous ablation) under the same condition of power delivery.

Detailed Description

The number of pulmonary vein isolation (PVI) therapy for atrial fibrillation (AF) is increasing. Durable PVI is cornerstone for long-term freedom of AF. In one previous study continuous ablation was suggested to be more efficient in durable PVI. However, this hypothesis has not been proven in randomized fashion. The current study is to confirm whether continuous versus discontinuous design of encircling lesions are comparable under the same conditions of power delivery. The study design is a two-centre prospective randomized trial to compare the acute efficacy by using the above described approaches.

Registry
clinicaltrials.gov
Start Date
September 15, 2017
End Date
January 31, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Institute for Clinical and Experimental Medicine
Responsible Party
Principal Investigator
Principal Investigator

Bashar Aldhoon

Dr. Bashar Aldhoon, PhD

Institute for Clinical and Experimental Medicine

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing pulmonary vein isolation with radiofrequency catheter ablation for paroxysmal atrial fibrillation treatment.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Combined unsuccessful PVI or PV reconnection

Time Frame: 30 min after ablation

Combined unsuccessfuk PVI after completeing the primary lesion set or PV reconnection during the waiting time

Secondary Outcomes

  • Early pulmunary veins reconnection(10 min.)

Study Sites (1)

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