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A Randomised Comparison of Left and Right Sided Approaches to Ablation of the Atrioventricular Junction

Not Applicable
Conditions
Atrial Fibrillation
Interventions
Procedure: atrioventricular node ablation
Registration Number
NCT05211453
Lead Sponsor
East Sussex Hospitals NHS Trust
Brief Summary

This study will compare right sided atrioventricular node ablation to left sided atrioventricular node ablation

Detailed Description

Right-sided atrioventricular node ablation has been the initial conventional approach however up to 18.5% of patients require switching to a left sided approach or have a challenging procedure. Previous studies have found that left sided ablation is more efficacious than right-sided ablation requiring less than 5 applications of radiofrequency energy to induce atrioventricular block.

This study will compare right sided atrioventricular node ablation to left sided atrioventricular node ablation

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Age greater than or equal to 18 years
  • Referred for atrioventricular node ablation for any such indication
Exclusion Criteria
  • Stroke or transient ischaemic attack (TIA) within 6 months
  • Myocardial infarction within 6 months
  • Medical conditions limiting expected survival to <1 year
  • Moderate to severe aortic stenosis
  • History of aortic or mitral valve replacement
  • Pregnancy or breast feeding women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Right sided atrioventricular node ablationatrioventricular node ablationRight sided atrioventricular node ablation
Left sided atrioventricular node ablationatrioventricular node ablationLeft sided atrioventricular node ablation
Primary Outcome Measures
NameTimeMethod
Comparison of total ablation time required to induce complete atrioventricular node blockintraoperative

Time in seconds

Secondary Outcome Measures
NameTimeMethod
Comparison of number of RF applications required to induce complete atrioventricular node blockintraoperative

Comparison of number of RF applications required to induce complete atrioventricular node block

Comparison of rate of the escape rhythm after ablation in beats/minintraoperative

Comparison of rate of the escape rhythm after ablation in beats/min

Comparison of number of patients requiring crossover to each sideintraoperative

Comparison of number of patients requiring crossover to each side

Comparison of adverse events / complications between each groupintraoperative

Comparison of adverse events / complications between each group

Comparison of total procedure time between the two groupsintraoperative

Comparison of total procedure time between the two groups

Comparison of radiation exposure between the two groupsintraoperative

Comparison of radiation exposure between the two groups

Comparison of patient comfort of procedureintraoperative

Comparison of patient comfort of procedure using visual analogue scale ( 0-100)

Trial Locations

Locations (1)

Eastbourne District General Hospital

🇬🇧

Eastbourne, East Sussex, United Kingdom

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