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ICE: Intracardiac Ultrasound Within the Left Atrium During Radiofrequency Ablation of Nonvalvular Atrial Fibrillation

G

Gregory Jones

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Device: Biosense Webster irrigated tip catheter
Procedure: Pulmonary vein isolation
Procedure: ICE catheter placed through one of two existing 8F sheaths

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

Imaging Real Time within the Left atrial chamber Enhances safety and efficacy of Radiofrequency Ablation of Atrial Fibrillation

Full description

Atrial fibrillation is the most common rhythm disturbance affecting the human population.

  1. Its prevalence increases with age and can be found in >8% of humans over the age of eighty;
  2. Radiofrequency ablation for drug refractory nonvalvular atrial fibrillation has become a common therapy available to patients. It has been shown to be both efficacious and cost effective;
  3. The standard approach to atrial fibrillation involves electrical isolation of the pulmonary veins (PVI) from the rest of the atrium chamber. This involves moving a 3.5mm tip ablation catheter point to point around the PV structures until an encircling ablation line is formed. This can be made difficult by not knowing if the tip is in good contact with the atrial tissue. In addition the esophagus is a posterior lying structure and injury to the esophagus by ablating the overlying tissue has been reported, at times fatal;
  4. Currently, intracardiac imaging of the left atrium has FDA approval in the right atrial chamber. This leads to difficulty in visualizing tip tissue interface, and important left sided structures such as carina, ligaments, and esophagus. By placing the tip of the ICE catheter in the left atrium, enhanced visualization of the tip tissue interface may lead to more effective ablation points, fewer needed ablation points, and enhanced safety by avoiding placement over adjacent noncardiac structures.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 to 80 years
  • Recommended for radiofrequency ablation of nonvalvular atrial fibrillation

Exclusion criteria

  • none

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Study arm
Experimental group
Description:
The study arm group will have the ICE catheter placed through one of two existing 8F sheaths already in the left atrium. The ICE catheter will be exchanged in the sheath utilizing the lasso multipolar mapping catheter during left pulmonary vein ablation lines. During exchange, suction and irrigation techniques will be utilized to avoid any air or thrombus embolization. All patients will have standard anticoagulation during the procedure with heparin infusion adjusted to an activated clotting time (ACT) of 350-400. The left sided ICE catheter will be adjusted to visualize left sided structures, ablation tip and tissue interface, and adjacent noncardiac structures such as the esophagus during radiofrequency ablation of the left pulmonary vein system.
Treatment:
Device: Biosense Webster irrigated tip catheter
Procedure: ICE catheter placed through one of two existing 8F sheaths
Device: Biosense Webster irrigated tip catheter
Control arm
Active Comparator group
Description:
The control arm group will receive standard pulmonary vein isolation (PVI) procedure utilizing intracardiac guided ultrasound (ICE) placed within the right atrium via the femoral vein.
Treatment:
Procedure: Pulmonary vein isolation
Device: Biosense Webster irrigated tip catheter
Device: Biosense Webster irrigated tip catheter

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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