Foresight Intracardiac Echocardiography System (ICE)

Conavi13 enrolled

Overview

This study will evaluate the efficacy of the Foresight Intracardiac Echocardiography system ,with improved image quality, in guiding trans-septal punctures during atrial fibrillation ablation procedures.

The study will recruit 10 patients at a single center.

Study Type

INTERVENTIONAL

Allocation

Purpose

DEVICE_FEASIBILITY

Masking

NONE

Enrollment

Conditions

Atrial Fibrillation

Interventions

Intracardiac echocardiography imagingDEVICE

Wide visualization of the the heart anatomy and additional devices used during atrial fibrillation ablation procedures.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient is at least 18 years old. * Patient is undergoing an atrial fibrillation ablation procedure. * Patient has a transesophageal echocardiogram (TEE) within the 48 hours prior to ablation procedure to rule out left atrial thrombus. * Patient provides informed, written consent for participation in the study. Exclusion Criteria: * Patients in whom placement of an ICE catheter in the right atrium for adequate atrial visualization is not technically feasible (as evaluated and determined by the physician/study investigator performing the procedure). * Patients in whom transseptal puncture is relatively contraindicated. * Patients in whom left atrial clot or dense spontaneous contrast is identified on TEE, which would increase thromboembolic risk. * Women of child bearing potential, in whom pregnancy cannot be excluded. * Patients unable to grant informed, written consent for participation in the study.

Locations (1)

Southlake Regional Health Centre

Newmarket, Ontario, Canada

Outcomes

Primary Outcomes

Evaluation of the study device for guiding transseptal puncture in order to gain access to the left atrium of the heart during an ablation procedure in patients suffering with atrial fibrillation.

The ability of the study device to identify the atrial septum during transseptal puncture will be evaluated by the physician on the day of the procedure and captured in the individual case report form. This will be based on the objective finding of whether the transseptal puncture was performed (Yes or No) under study device guidance. This information will be gathered for each patient in the individual case report form and presented qualitatively and as quantitative measures (percentage success).

Time frame: For each patient, the individual physician satisfaction survey will be completed on the day of the procedure.

Secondary Outcomes

Collection of first human images with Conavi's Foresight System.

The Conavi's Foresight System will be utilized to capture images of relevant human cardiac anatomical landmarks (e.g. crista terminalis, tricuspid valve, coronary sinus) while the catheter will be manipulated inside the heart during the procedure. The physician satisfaction survey will ask the physician to specifically tabulate structures that could be identified in a binary yes/no format. This kind of information will be gathered for each patient in the individual physician satisfaction surveys and presented qualitatively.

Time frame: An individual physician satisfaction survey will be completed for each case on the day of the procedure.

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.