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Clinical Trials/NCT03242941
NCT03242941
Completed
Not Applicable

AF Septal Pacing (Clinical Investigation Plan)

Medtronic BRC3 sites in 2 countries16 target enrollmentApril 26, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Paroxysmal Atrial Fibrillation
Sponsor
Medtronic BRC
Enrollment
16
Locations
3
Primary Endpoint
Number of Electrodes in a Stable Position
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this non-randomized, non-controlled, acute, single-arm research study is to evaluate the feasibility to obtain a stable position of a ring of stimulation electrodes on the interatrial septum. The possibility to terminate atrial arrythmias will also be evaluated.

Detailed Description

The evidence of treating AF by pacing is limited, although these algorithms are of interest, since they appear to be safe and usually add little additional cost. Using a computer model, a new dual-stage septal pacing has been developed.The proposed septal pacing algorithm could suppress AF reentries in a more robust way than classical single site rapid pacing. The feasibility of pacing both atria simultaneously from a single lead placed in the interatrial septum has been previously demonstrated clinically. The septal pacing concept has also been successfully tested in a computer model of AF and in a pig model . Experimental studies are now needed to determine whether similar termination mechanisms and efficacies can be observed in humans. The purpose of this non-randomized, non-controlled, acute, single-arm research study is to evaluate the feasibility to obtain a stable position of a ring of stimulation electrodes on the interatrial septum

Registry
clinicaltrials.gov
Start Date
April 26, 2018
End Date
December 21, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Medtronic BRC
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient referred to the center to undergo ablation of the pulmonary vein using radiofrequency (initial AF ablation, or redo procedure).
  • In case of paroxysmal AF the right atrium should be dilated as indicated by \> 29 ml mm2 or the left atrium should be dilated as indicated by \> 34 ml mm
  • Patient is willing and able to cooperate with the study procedure.
  • Patient is willing to provide the Informed Consent for their participation in the study.

Exclusion Criteria

  • Patients under 18 years or over 80 years old.
  • Women who are currently pregnant or have a positive pregnancy test.
  • Patients with an implantable cardiac device.
  • Patients who already underwent an AF septal ablation procedure.

Outcomes

Primary Outcomes

Number of Electrodes in a Stable Position

Time Frame: 30 minutes

To assess Pacing Site Stability, the number of interatrial septal pacing electrodes which are successfully placed in a stable position, will be counted. A stable position in this study is defined as a location where the pacing threshold will be \< 10 mA at a pacing pulse width of 1 msec. Stable pacing further requires that no ventricular capture will be induced during atrial stimulation at twice the atrial capture threshold.

Secondary Outcomes

  • Localized Atrial Capture(30 minutes)
  • Termination of Atrial Tachyarrhythmia.(30 minutes)

Study Sites (3)

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