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AF Septal Pacing (Clinical Investigation Plan)

AF Septal Pacing (Clinical Investigation Plan)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03242941
Enrollment
16
Registered
2017-08-08
Start date
2018-04-26
Completion date
2018-12-21
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation

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

Interventions

After pulmonary vein isolation, during the routine waiting time of half an hour to confirm efficacy of the ablation, the septal catheter, already in place in right atrium, will be positioned on the interatrial septum. If the patient will not be in sinus rhythm, he/she will be externally cardioverted in order to determine pacing thresholds and impedances on all septal catheter electrodes. Next, atrial fibrillation will be induced by rapid atrial pacing.AF cycle length will be determined in the left atrial appendage, during 1 minute of atrial fibrillation using ablation catheter electrodes. Subsequently, a pacing scheme will be applied and capture on decapolar recording catheters, already in place for the standard ablation procedure will be assessed as well as AF termination.

Sponsors

Medtronic BRC
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Approximately 15 subjects with AF indicated for ablation of the pulmonary vein will be enrolled in the study. Participants will attend the Baseline visit and the Procedure visit. The baseline visit can be on the same day as the ablation procedure. Since it is an acute study, no follow-up visit will occur. The research procedure will be performed during an already scheduled ablation procedure. Subjects will be enrolled over a period of approximately 18 months

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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 mm2. * 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.

Design outcomes

Primary

MeasureTime frameDescription
Number of Electrodes in a Stable Position30 minutesTo 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

MeasureTime frameDescription
Localized Atrial Capture30 minutesTo assess Localized Atrial Capture the following endpoints will be considered: \- the number of AF episodes in which local capture is recorded during atrial septal stimulation in at least one of the electrode positions
Termination of Atrial Tachyarrhythmia.30 minutesTermination of atrial tachyarrhythmia.

Countries

Hungary, Netherlands

Participant flow

Pre-assignment details

If the pulmonary vein ablation succeeded and the subject was in sinus rhythm the study procedure started from the electrode testing. Alternatively, if the subject was still in AF, the electrode testing was performed after either the application of the dual stage pacing algorithm or the cardioversion, when the sinus rhythm was established.

Participants by arm

ArmCount
Paroxymal and Persistent AF Patients
Patients with either paroxymal or persistent AF already referred to the center for Pulmonary Vein Ablation will be stimulated delivering a novel dual-stage pacing protocol to terminate atrial fibrillation. Pulmonary vein ablation: After pulmonary vein isolation, during the routine waiting time of half an hour to confirm efficacy of the ablation, the septal catheter, already in place in right atrium, will be positioned on the interatrial septum. If the patient will not be in sinus rhythm, he/she will be externally cardioverted in order to determine pacing thresholds and impedances on all septal catheter electrodes. Next, atrial fibrillation will be induced by rapid atrial pacing.AF cycle length will be determined in the left atrial appendage, during 1 minute of atrial fibrillation using ablation catheter electrodes. Subsequently, a pacing scheme will be applied and capture on decapolar recording catheters will be assessed as well as AF termination.
14
Total14

Baseline characteristics

CharacteristicParoxymal and Persistent AF Patients
Age, Continuous55 years
STANDARD_DEVIATION 13
Height182 cm
STANDARD_DEVIATION 14
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
14 Participants
Sex: Female, Male
Female
2 Participants
Sex: Female, Male
Male
12 Participants
Weight92 kg
STANDARD_DEVIATION 20

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 14
other
Total, other adverse events
1 / 14
serious
Total, serious adverse events
0 / 14

Outcome results

Primary

Number of Electrodes in a Stable Position

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.

Time frame: 30 minutes

Population: The maximum number of electrode pairs used and potentially stable

ArmMeasureValue (COUNT_OF_UNITS)
Paroxymal and Persistent AF PatientsNumber of Electrodes in a Stable Position38 Electrode pairs
Secondary

Localized Atrial Capture

To assess Localized Atrial Capture the following endpoints will be considered: \- the number of AF episodes in which local capture is recorded during atrial septal stimulation in at least one of the electrode positions

Time frame: 30 minutes

Population: Patient treated with the new pacing scheme algorithm

ArmMeasureValue (COUNT_OF_UNITS)
Paroxymal and Persistent AF PatientsLocalized Atrial Capture8 Episodes
Secondary

Termination of Atrial Tachyarrhythmia.

Termination of atrial tachyarrhythmia.

Time frame: 30 minutes

Population: Patients treated with the new dual stage pacing algorithm

ArmMeasureValue (COUNT_OF_UNITS)
Paroxymal and Persistent AF PatientsTermination of Atrial Tachyarrhythmia.3 AF termination occurrence

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026