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A Trial of High Power-Short Duration Versus Standard Power-Long Duration Radiofrequency Ablation for Treatment of Atrial Fibrillation (Short-AF)

Primary Purpose

Atrial Fibrillation, Atrial Fibrillation Paroxysmal, Atrial Fibrillation, Persistent

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Catheter ablation with Standard RF ablation settings
Catheter ablation with High Power Short Duration RF ablation settings
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Atrial Fibrillation

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or female ≥18 years of age at their pre-operative visit.
  2. Patient is scheduled to have their first AF ablation
  3. Paroxysmal or persistent AF
  4. Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study.

Exclusion Criteria:

  1. Prior AF ablation
  2. Stroke or transient ischemic attack (TIA) within the previous 6 months
  3. Known esophageal ulcer or gastrointestinal (GI) bleed within prior 6 months
  4. Intent to perform adjunctive left atrial ablation, including posterior wall isolation, left atrial appendage isolation, mitral or other linear lesions.
  5. Prior rheumatic heart disease or significant mitral stenosis
  6. Mechanical mitral valve replacement
  7. Long lasting persistent AF > 1 year
  8. Severe left ventricular systolic dysfunction, with LV ejection fraction LVEF<35%
  9. Prior left atrial appendage (LAA) occlusion device
  10. Prior septal occlusion device
  11. Pregnancy
  12. Pacemaker, defibrillator or any contraindication to MRI

Sites / Locations

  • University of California, San Francisco

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard Catheter Settings

High Power Short Duration (HPSD)

Arm Description

Group 1 - Standard RF ablation settings

Group 2 - High power short duration RF

Outcomes

Primary Outcome Measures

Ablation Duration
RF ablation duration from start of first pulmonary vein isolation lesion to end of last lesion

Secondary Outcome Measures

Maximum esophageal temperature
Maximum esophageal temperature rise
Freedom from Atrial Fibrillation
>30 secs using Ziopatch, 1 year off or on previously ineffective antiarrhythmic drugs (AADs)
Freedom from Atrial Fibrillation
>30 secs using Ziopatch, 1 year off previously ineffective antiarrhythmic drugs (AADs)
% pulmonary vein pairs isolated with first encirclement
Number of radiofrequency lesions required for isolation/PV
Total left atrial radiofrequency (RF) time
Total procedure duration
Overall complication rate
Pleurisy
Pericardial effusion>1cm
Pericardial tamponade requiring drainage
Total saline infused
Presence of asymptomatic cerebral emboli

Full Information

First Posted
October 30, 2019
Last Updated
August 14, 2023
Sponsor
University of California, San Francisco
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1. Study Identification

Unique Protocol Identification Number
NCT04148664
Brief Title
A Trial of High Power-Short Duration Versus Standard Power-Long Duration Radiofrequency Ablation for Treatment of Atrial Fibrillation
Acronym
Short-AF
Official Title
SHORT-AF: A Randomized Trial of High Power-Short Duration Versus Standard Power-Long Duration Radiofrequency Ablation for Treatment of Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
December 3, 2019 (Actual)
Primary Completion Date
December 1, 2020 (Actual)
Study Completion Date
December 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco

4. Oversight

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

5. Study Description

Brief Summary
This study is a prospective, randomized controlled study to compare overall clinical outcomes between High Power Short Duration (HPSD) and standard radiofrequency (RF) ablation settings for Atrial Fibrillation (AF) ablation in the treatment of subjects with paroxysmal or persistent Atrial Fibrillation.
Detailed Description
Pulmonary vein isolation using radiofrequency (RF) ablation is a widely used treatment strategy for atrial fibrillation. Peri-procedural complications rates are estimated at between 1.5 - 6% with the two most feared complications being stroke and atrial-esophageal fistula. The risk of these complications increases with (1) longer left atrial dwell times with greater potential for clot formation and (2) esophageal heating during delivery of radiofrequency energy. 'High-power short-duration' (HPSD) is an increasingly utilized strategy to decrease procedure duration and minimize the risk of these complications. Potential mechanisms for benefit include: (1) shorter left atrial dwell times due to more efficient lesion delivery (2) rapid, but more controlled, resistive tissue heating, which avoids deeper, passive conductive heating that can reach the esophagus and cause injury. Moreover, HPSD may improve lesion efficacy and durability due to less recover of excitability after ablation. Despite being widely used and several retrospective studies, there have been no prospective randomized trials comparing outcomes between HPSD and standard RF ablation settings. Moreover, the investigators are interested to see if a shorter procedure (less time in the left atrium) is associated with a lower rate of silent cerebral infarctions (which are occasionally seen on MRI brain post RF ablation - their clinical significance is unclear).

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a multi-center prospective single-blinded randomized controlled trial. Enrollment of 60 subjects undergoing clinically-indicated AF ablation is planned with 1:1 block randomization (standard 'low power' RF settings n=30, HPSD n=30 and allowing for 10 drop-outs / consent withdrawals). Follow-up will be over 12 months.
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Catheter Settings
Arm Type
Active Comparator
Arm Description
Group 1 - Standard RF ablation settings
Arm Title
High Power Short Duration (HPSD)
Arm Type
Experimental
Arm Description
Group 2 - High power short duration RF
Intervention Type
Procedure
Intervention Name(s)
Catheter ablation with Standard RF ablation settings
Intervention Description
Standard RF ablation settings (n=30): Maximum 35W for 20-40 seconds, per operator standard.
Intervention Type
Procedure
Intervention Name(s)
Catheter ablation with High Power Short Duration RF ablation settings
Intervention Description
High power short duration RF (n=30): Maximum 50 Watts for 5-15 seconds, per operator standard.
Primary Outcome Measure Information:
Title
Ablation Duration
Description
RF ablation duration from start of first pulmonary vein isolation lesion to end of last lesion
Time Frame
During Ablation
Secondary Outcome Measure Information:
Title
Maximum esophageal temperature
Time Frame
During ablation
Title
Maximum esophageal temperature rise
Time Frame
During ablation
Title
Freedom from Atrial Fibrillation
Description
>30 secs using Ziopatch, 1 year off or on previously ineffective antiarrhythmic drugs (AADs)
Time Frame
assessed at 6 and 12 months post-ablation
Title
Freedom from Atrial Fibrillation
Description
>30 secs using Ziopatch, 1 year off previously ineffective antiarrhythmic drugs (AADs)
Time Frame
assessed at 6 and 12 months post-ablation
Title
% pulmonary vein pairs isolated with first encirclement
Time Frame
During Ablation
Title
Number of radiofrequency lesions required for isolation/PV
Time Frame
During Ablation
Title
Total left atrial radiofrequency (RF) time
Time Frame
During Ablation
Title
Total procedure duration
Time Frame
During Ablation
Title
Overall complication rate
Time Frame
During Ablation and up to 12 month follow up assessment
Title
Pleurisy
Time Frame
At 1 week and 1 month assessment
Title
Pericardial effusion>1cm
Time Frame
During ablation or up to 30 days post ablation
Title
Pericardial tamponade requiring drainage
Time Frame
During ablation or up to 30 days post ablation
Title
Total saline infused
Time Frame
During Ablation
Title
Presence of asymptomatic cerebral emboli
Time Frame
1 day post-ablation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female ≥18 years of age at their pre-operative visit. Patient is scheduled to have their first AF ablation Paroxysmal or persistent AF Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study. Exclusion Criteria: Prior AF ablation Stroke or transient ischemic attack (TIA) within the previous 6 months Known esophageal ulcer or gastrointestinal (GI) bleed within prior 6 months Intent to perform adjunctive left atrial ablation, including posterior wall isolation, left atrial appendage isolation, mitral or other linear lesions. Prior rheumatic heart disease or significant mitral stenosis Mechanical mitral valve replacement Long lasting persistent AF > 1 year Severe left ventricular systolic dysfunction, with LV ejection fraction LVEF<35% Prior left atrial appendage (LAA) occlusion device Prior septal occlusion device Pregnancy Pacemaker, defibrillator or any contraindication to MRI
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edward P Gerstenfeld, MD
Organizational Affiliation
Chief of Cardiac Electrophysiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We are open to collaboration but do not plan to give our data to others.
Citations:
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A Trial of High Power-Short Duration Versus Standard Power-Long Duration Radiofrequency Ablation for Treatment of Atrial Fibrillation

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