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Unexcitability Along the Ablation as an Endpoint for Atrial Fibrillation Ablation

U

Universitätsklinikum Hamburg-Eppendorf

Status

Completed

Conditions

Paroxysmal Atrial Fibrillation
Catheter Ablation Strategies

Treatments

Device: catheter based pulmonary vein isolation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

to assess the near-term (12 months) efficacy of pulmonary vein isolation.

Full description

The aim of the study was to assess the near-term (12 months) efficacy of pulmonary vein isolation using a standard approach compared to application of an additional acute procedural endpoint of unexcitability along the ablation line.

Enrollment

102 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • written informed consent
  • age > 18 years
  • paroxysmal atrial fibrillation

Exclusion criteria

  • structural heart disease
  • intracardiac thrombus
  • reversible causes of atrial fibrillation
  • inability to take warfarin

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Loss of pace capture
Active Comparator group
Description:
Pulmonary vein isolation: Ablation along the ablation line is continued until loss of pace capture along the ablation line is achieved catheter based pulmonary vein isolation
Treatment:
Device: catheter based pulmonary vein isolation
Conventional
Active Comparator group
Description:
Pulmonary vein isolation: Ablation is discontinued when electrical isolation of the pulmonary veins is achieved. catheter based pulmonary vein isolation
Treatment:
Device: catheter based pulmonary vein isolation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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