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Ablation of Low Voltage Regions in Persistent Atrial Fibrillation (ABLOVO-AF)

Primary Purpose

Persistent Atrial Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Low voltage ablation
Pulmonary Vein Isolation
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Atrial Fibrillation focused on measuring Radiofrequency Catheter Ablation

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Suitable candidate for catheter mapping/ablation for arrhythmias.
  2. Eighteen (18) to eighty-five (85) years of age
  3. Body Mass Index (BMI) < 40 (Wt. in Kgs / Ht. in m2)
  4. Signed Informed Consent

Exclusion Criteria:

  1. Severe cerebrovascular disease
  2. Moderate to severe renal impairment (eGFR < 30)
  3. Active gastrointestinal bleeding
  4. Active infection or fever
  5. Short life expectancy
  6. Significant anemia
  7. Severe uncontrolled systemic hypertension
  8. Severe electrolyte imbalance
  9. Ejection fraction of < 35%
  10. Congestive heart failure (NYHA Class IV)
  11. Unstable angina requiring emergent PTCA (percutaneous transluminal coronary angioplasty) or CABG (coronary artery bypass graft)
  12. Recent myocardial infarction
  13. Bleeding or clotting disorders
  14. Uncontrolled diabetes
  15. Inability to receive IV or oral Anticoagulants
  16. Unable to give informed consent (these patients would not be recruited)
  17. Previous catheter or surgical ablation treatment for atrial fibrillation.
  18. Paroxysmal atrial fibrillation.
  19. Pregnancy (urinary pregnancy test will be offered on the day of the procedure for all women of reproductive age)
  20. Drug and/or alcohol abuse
  21. Transient factors for AF
  22. Severe LA enlargement of >60 mm in diameter on echocardiography
  23. Patients who have participated in another study of an investigational medicinal product in the last 3 months.

Sites / Locations

  • Hammersmith HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Pulmonary Vein Isolation

Low voltage ablation

Arm Description

Historical control from cases performed in year 2017 at Hammersmith Hospital. Intervention: Pulmonary vein isolation.

Active arm, Intervention: Standard pulmonary vein isolation and Low Voltage Ablation.

Outcomes

Primary Outcome Measures

Atrial fibrillation recurrence
Recurrence of atrial arrhythmia of at least 30s in duration. Investigation period for arrhythmia recurrence will be between 3 and 12 months after the first procedure, allowing for a blanking period of 3 months.

Secondary Outcome Measures

Canadian Cardiovascular Society Severity in Atrial Fibrillation Score
Canadian Cardiovascular Society Severity in Atrial Fibrillation (CCS-SAF) change. 0 represents no symptoms, 4 represents symptoms that significantly interfere with quality of life and exercise capacity.
Antiarrhythmic drugs
Change in the number of antiarrhythmic drugs per patient
Number of AF ablations
Number of additional AF ablations
Complication rate
Number and rate of complications in the study population.

Full Information

First Posted
January 18, 2019
Last Updated
January 28, 2019
Sponsor
Imperial College London
Collaborators
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT03811938
Brief Title
Ablation of Low Voltage Regions in Persistent Atrial Fibrillation
Acronym
ABLOVO-AF
Official Title
Catheter ABlation of Low Voltage Regions in the Treatment of Persistent Atrial Fibrillation (ABLOVO-AF Study)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 24, 2017 (Actual)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London
Collaborators
Abbott

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
Background. Atrial fibrillation (AF) is a disorganised rhythm of the upper chambers of the heart. It can lead to severe complications including stroke or heart failure. It can be treated with radiofrequency ablation (RFA). This technology works by heating heart muscle inside the heart to break the electrical circuits responsible for the abnormal rhythm. The energy is delivered into the heart with plastic tubes that have metal electrodes, inserted through the groin veins and removed after the procedure. The patient is usually put to sleep during the intervention. If the AF has been present for more than seven days but for less than one year it is called persistent, and it can be difficult to treat successfully with the usual methods. Goals. The study will test a new RFA technique to treat patients with persistent AF. This involves identifying areas within the left upper chamber that have a lower electrical voltage than the surrounding heart muscle and applying RFA to the border zones of these areas. Methods. The new technology combined with the usual procedure will be compared to the usual procedure alone. All patients will receive ablation according to the new technique and results will be compared to a historical control group from the trial institution. Follow up. Patients will be followed up for 12 months with clinic visits and heart rhythm checks. Potential benefit. The new technique will be assessed for success at keeping patients free from persistent AF compared to the usual methods. The study will be performed at Imperial College Healthcare NHS Trust, at the Hammersmith Hospital. Licensed clinical software will be used from St Jude Medical to guide ablation and a special research software module will be used to analyse data from the heart following ablation. The study will be sponsored by Imperial College Healthcare NHS Trust

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Atrial Fibrillation
Keywords
Radiofrequency Catheter Ablation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pulmonary Vein Isolation
Arm Type
Active Comparator
Arm Description
Historical control from cases performed in year 2017 at Hammersmith Hospital. Intervention: Pulmonary vein isolation.
Arm Title
Low voltage ablation
Arm Type
Experimental
Arm Description
Active arm, Intervention: Standard pulmonary vein isolation and Low Voltage Ablation.
Intervention Type
Procedure
Intervention Name(s)
Low voltage ablation
Intervention Description
Catheter ablation of low voltage areas in the left atrium and catheter ablation aiming for the electrical isolation of the pulmonary veins.
Intervention Type
Procedure
Intervention Name(s)
Pulmonary Vein Isolation
Intervention Description
Catheter ablation aiming for the electrical isolation of the pulmonary veins.
Primary Outcome Measure Information:
Title
Atrial fibrillation recurrence
Description
Recurrence of atrial arrhythmia of at least 30s in duration. Investigation period for arrhythmia recurrence will be between 3 and 12 months after the first procedure, allowing for a blanking period of 3 months.
Time Frame
3-12 months.
Secondary Outcome Measure Information:
Title
Canadian Cardiovascular Society Severity in Atrial Fibrillation Score
Description
Canadian Cardiovascular Society Severity in Atrial Fibrillation (CCS-SAF) change. 0 represents no symptoms, 4 represents symptoms that significantly interfere with quality of life and exercise capacity.
Time Frame
12 months
Title
Antiarrhythmic drugs
Description
Change in the number of antiarrhythmic drugs per patient
Time Frame
3-12 months
Title
Number of AF ablations
Description
Number of additional AF ablations
Time Frame
3-12 months
Title
Complication rate
Description
Number and rate of complications in the study population.
Time Frame
3-12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Suitable candidate for catheter mapping/ablation for arrhythmias. Eighteen (18) to eighty-five (85) years of age Body Mass Index (BMI) < 40 (Wt. in Kgs / Ht. in m2) Signed Informed Consent Exclusion Criteria: Severe cerebrovascular disease Moderate to severe renal impairment (eGFR < 30) Active gastrointestinal bleeding Active infection or fever Short life expectancy Significant anemia Severe uncontrolled systemic hypertension Severe electrolyte imbalance Ejection fraction of < 35% Congestive heart failure (NYHA Class IV) Unstable angina requiring emergent PTCA (percutaneous transluminal coronary angioplasty) or CABG (coronary artery bypass graft) Recent myocardial infarction Bleeding or clotting disorders Uncontrolled diabetes Inability to receive IV or oral Anticoagulants Unable to give informed consent (these patients would not be recruited) Previous catheter or surgical ablation treatment for atrial fibrillation. Paroxysmal atrial fibrillation. Pregnancy (urinary pregnancy test will be offered on the day of the procedure for all women of reproductive age) Drug and/or alcohol abuse Transient factors for AF Severe LA enlargement of >60 mm in diameter on echocardiography Patients who have participated in another study of an investigational medicinal product in the last 3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Szabolcs Nagy, MD
Phone
447821694566
Email
s.nagy@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Phang B Lim, MB BChir
Organizational Affiliation
Imperial College Healthcare NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hammersmith Hospital
City
London
ZIP/Postal Code
W12 0HS
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Szabolcs Nagy, MD
Phone
447821694566
Email
s.nagy@nhs.net

12. IPD Sharing Statement

Plan to Share IPD
No

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Ablation of Low Voltage Regions in Persistent Atrial Fibrillation

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