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Subclavian Ansae Stimulation in AF (SAS-AF) ((SAS-AF))

Primary Purpose

Atrial Fibrillation

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Selective left subclavian ansae stimulation
Sponsored by
Barts & The London NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Atrial Fibrillation focused on measuring Atrial Fibrillation, Subclavian ansae stimulation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ability to give informed consent
  • Age 18-80 years
  • First time PAF ablation

Exclusion Criteria:

  • Creatinine clearance (eGFR) < 30mls/min
  • Contraindication or unable to take anticoagulation
  • Uncontrolled hypertension
  • Contraindication for catheter ablation
  • BMI > 35
  • Haemodynamically unstable
  • Recent Stroke/ myocardial infarction
  • Significant carotid artery stenosis
  • Significant carotid artery stenosis or peripheral arterial disease
  • Allergy to contrast
  • Presence of pacemaker or implantable cardioverter defibrillator (ICD)

Sites / Locations

  • Barts Heart CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Participants will receive stimulation of the left subclavian ansae.

Arm Description

Participants as self-controlled cases for the study. Human cardiac haemodynamics and electrophysiological in response to left subclavian ansae stimulation will be studied.

Outcomes

Primary Outcome Measures

Measuring the rate of change in heart rate (beats per minute) in response to subclavian ansae stimulation (SAS).
Measuring the change in heart rate during and post stimulation of the SAS compared to baseline measurement at rest through the mapping catheter and surface ECG electrodes.
Measuring the rate of change in blood pressure (mmHg) in response to subclavian ansae stimulation (SAS).
Measuring the blood pressure (systolic and diastolic) through the arterial line during and post stimulation of the SAS compared to baseline measurements at rest.
Measuring the rate of change in conduction velocity (m/s) within left and right atrium in response to subclavian ansae stimulation (SAS).
Measuring the conduction velocity in each atrium and changes between the atrial conduction using the intra cardiac catheter electrodes post SAS stimulation comparing with baseline measurements at rest.
Measuring the rate of change in action potential duration (ms) and effective refractive period (ms) in response to subclavian ansae stimulation (SAS).
Measurements taken in both atria using the intra cardiac catheter electrodes post SAS stimulation compared to baseline measurements at rest.
Proportion of participants where AF is inducible in response to Subclavian ansae stimulation
Number of participants where AF is inducible in response to selective left subclavian ansae stimulation.

Secondary Outcome Measures

Determining the optimal output threshold (Volts/Kg) to selectively stimulate left subclavian ansae via the subclavian artery
To determine the delivery energy to stimulate the subclavian ansae to achieve 10-20% increase in heart rate from baseline with stimulation in each participants.
Safety and procedure specific complications
To assess procedure specific complications related to subclavian ansae stimulation

Full Information

First Posted
November 1, 2021
Last Updated
July 19, 2023
Sponsor
Barts & The London NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT05133414
Brief Title
Subclavian Ansae Stimulation in AF (SAS-AF)
Acronym
(SAS-AF)
Official Title
Effects of Selective Left Subclavian Ansae Stimulation on Human Cardiac Electrophysiological Properties - a Potential Percutaneous Target for Neuromodulation in Atrial Fibrillation.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 5, 2022 (Actual)
Primary Completion Date
January 4, 2024 (Anticipated)
Study Completion Date
January 4, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barts & The London NHS Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Atrial Fibrillation (AF) is a common heart rhythm condition that affects over 3% of the total population. AF can lead to serious health problems such as heart failure or stroke and can also cause troublesome symptoms in some people. Although many advances have been made, there remains a pressing need to improvement treatment of AF. It is increasingly recognised that the brain and nerves can influence the electrical activity of the heart. Therefore, this research involves studying a new nerve target (Subclavian ansae) that is connected to the heart and can be a potential target for future treatment of AF. This nerve lies around an area close to an artery that runs to participant's left arm called left subclavian artery which can be approached via leg (key hole). The investigators aim to conduct this study in patients who have been referred for first time AF ablation.
Detailed Description
Atrial Fibrillation (AF) is a common and significant medical problem that affects approximately 3% of the population. There is increasing recognition of the importance of interactions between the heart and the autonomic nervous system (ANS) in the pathophysiology of arrhythmias. The role of ANS in the onset and maintenance of AF is thought to be related to autonomic imbalance. Several studies have experimented the use of autonomic modification in AF and identified potential targets for therapy ( for example: ganglionic plexi ablation, renal denervation, stellate ganglion block, and low level vagal nerve stimulation). However, some targets like stellate ganglion block/sympathectomy will have off-target side-effects. Easily accessible, minimally invasive, and selective targets for neuromodulation are of great interest for development of novel therapy in the management of AF. The subclavian ansae was first described in 1864 by Vieussens and is a nerve cord that forms a loop inferiorly around the subclavian artery and connects the inferior cervical ganglion and middle cervical ganglia.According to literature cardiac-related preganglionic fibers arising from the thoracic cord traverse up the paravertebral chain through the T1-T2 region, some making synaptic contact with postganglionic neurons in the stellate with others projecting through the subclavian ansae to more distal intrathoracic ganglia (middle cervical, mediastinal, and intrinsic). As such the ansa subclavia and the T1-T2 region of the paravertebral chain are critical nexus points for sympathetic nerve traffic to and afferent projections of the heart. Based on structure and function consideration, both sites are potential targets for cardiac neuromodulation. Preclinical studies have showed that stimulation of the subclavian ansae produces reproducible increases in cardiac rate, contractility and conduction velocity. Denervation of the subclavian ansae followed by stellate ganglion stimulation results in no change in cardiac indices confirming the nodal intervention point for cardiac sympathetic traffic. Due to the close anatomical proximity, stimulation of subclavian ansae should be possible via the subclavian artery which is accessible by percutaneous approach. Hypothesis: The investigators intend to introduce a percutaneous approach for identification and stimulation of subclavian ansae (sympathetic nerves) which exclusively innervate the heart and therefore stimulation will result in in changes in human cardiac haemodynamic and electrophysiological parameters. Primary objective: The primary objective of the study is to determine the human cardiac haemodynamics and electrophysiological response to left subclavian ansae stimulation (SAS) in patients with AF. Secondary objective: To determine appropriate stimulation parameters to selectively target subclavian ansae via percutaneous transarterial approach and to confirm safety of the procedure. Patients referred by Electrophysiologist for catheter ablation of paroxysmal AF (PAF) will be recruited. Participants will undergo consenting for the procedure and their involvement in the research study. The procedure will be performed under general anaesthesia. A stimulation wire will be passed into the left subclavian artery via the femoral arterial access. Further wires will be passed (via venous access) to the left top chamber of the heart which will then be used for 3D guided AF ablation after stimulation protocol. Study measurements will be gathered before and after the stimulation subclavian ansae. This will be followed by AF ablation (pulmonary vein isolation) and direct current cardioversion (DCCV) [if required] as standard care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Atrial Fibrillation, Subclavian ansae stimulation

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Participants will receive stimulation of the left subclavian ansae.
Arm Type
Experimental
Arm Description
Participants as self-controlled cases for the study. Human cardiac haemodynamics and electrophysiological in response to left subclavian ansae stimulation will be studied.
Intervention Type
Other
Intervention Name(s)
Selective left subclavian ansae stimulation
Intervention Description
Percutaneous, transarterial approach for target stimulation
Primary Outcome Measure Information:
Title
Measuring the rate of change in heart rate (beats per minute) in response to subclavian ansae stimulation (SAS).
Description
Measuring the change in heart rate during and post stimulation of the SAS compared to baseline measurement at rest through the mapping catheter and surface ECG electrodes.
Time Frame
During index procedure for catheter ablation
Title
Measuring the rate of change in blood pressure (mmHg) in response to subclavian ansae stimulation (SAS).
Description
Measuring the blood pressure (systolic and diastolic) through the arterial line during and post stimulation of the SAS compared to baseline measurements at rest.
Time Frame
During index procedure for catheter ablation
Title
Measuring the rate of change in conduction velocity (m/s) within left and right atrium in response to subclavian ansae stimulation (SAS).
Description
Measuring the conduction velocity in each atrium and changes between the atrial conduction using the intra cardiac catheter electrodes post SAS stimulation comparing with baseline measurements at rest.
Time Frame
During index procedure for catheter ablation
Title
Measuring the rate of change in action potential duration (ms) and effective refractive period (ms) in response to subclavian ansae stimulation (SAS).
Description
Measurements taken in both atria using the intra cardiac catheter electrodes post SAS stimulation compared to baseline measurements at rest.
Time Frame
During index procedure for catheter ablation
Title
Proportion of participants where AF is inducible in response to Subclavian ansae stimulation
Description
Number of participants where AF is inducible in response to selective left subclavian ansae stimulation.
Time Frame
During index procedure for catheter ablation
Secondary Outcome Measure Information:
Title
Determining the optimal output threshold (Volts/Kg) to selectively stimulate left subclavian ansae via the subclavian artery
Description
To determine the delivery energy to stimulate the subclavian ansae to achieve 10-20% increase in heart rate from baseline with stimulation in each participants.
Time Frame
During index procedure for catheter ablation
Title
Safety and procedure specific complications
Description
To assess procedure specific complications related to subclavian ansae stimulation
Time Frame
During index procedure for catheter ablation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ability to give informed consent Age 18-80 years First time PAF ablation Exclusion Criteria: Creatinine clearance (eGFR) < 30mls/min Contraindication or unable to take anticoagulation Uncontrolled hypertension Contraindication for catheter ablation BMI > 35 Haemodynamically unstable Recent Stroke/ myocardial infarction Significant carotid artery stenosis Significant carotid artery stenosis or peripheral arterial disease Allergy to contrast Presence of pacemaker or implantable cardioverter defibrillator (ICD)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Malcolm Finlay
Phone
02037658635
Email
malcolm.finlay1@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Vijayabharathy Kanthasamy
Phone
02037658635
Email
vijayabharathy.kanthasamy@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malcolm Finlay
Organizational Affiliation
Barts Heart Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barts Heart Centre
City
London
ZIP/Postal Code
EC1A 7BE
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Malcolm Finlay, PhD FRCP
Phone
02037658635
Email
malcolm.finlay1@nhs.net
First Name & Middle Initial & Last Name & Degree
Richard Ang, PhD FRCP
Phone
02037658635
Email
richard.ang@nhs.net
First Name & Middle Initial & Last Name & Degree
Malcolm Finlay, PhD FRCP
First Name & Middle Initial & Last Name & Degree
Richard Ang, PhD FRCP
First Name & Middle Initial & Last Name & Degree
Vijayabharathy Kanthasamy, MBBS MRCP

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The data will be anonymous

Learn more about this trial

Subclavian Ansae Stimulation in AF (SAS-AF)

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