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High Intensity Focused Ultrasound (HIFU) Ablation System Study

Primary Purpose

Atrial Fibrillation

Status
Suspended
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
propafenone
flecainide
dofetilide
sotolol
Pulmonary vein ablation
Amiodarone
Sponsored by
ProRhythm, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring atrial fibrillation, arrhythmia, AF ablation, antiarrhythmic agent, catheter ablation, pulmonary veins

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Documented atrial fibrillation
  • Failed or intolerant to at least 1 anti-arrhythmic drug
  • Able to take anti-coagulant therapy
  • Able to complete screening tests required for inclusion/exclusion criteria
  • Able to take at least 1 approved anti-arrhythmic drug
  • Not pregnant
  • Available for follow-up for at least 12 months

Exclusion Criteria:

  • Persistent or permanent atrial fibrillation
  • Mitral disease
  • Prior surgical treatment for atrial fibrillation
  • Ablation for treatment of atrial fibrillation within 6 months
  • Severe left ventricular hypertrophy
  • Known untreated coagulopathy
  • Unstable angina
  • Prior stroke
  • Uncontrolled heart failure
  • Secondary causes of atrial fibrillation
  • Uncorrected hyperthyroidism within 12 months
  • Pulmonary embolism within 6 months
  • Pneumonia or acute pulmonary disease within 3 months
  • Pacemaker/ICD
  • High risk for esophageal disease
  • Currently enrolled in investigational drug or device study

Sites / Locations

  • Fullerton Vascular Medical Group
  • University of California, Los Angeles
  • Piedmont Hospital
  • Lexington Central Baptist Hospital
  • Johns Hopkins Hopsital
  • Lahey Clinic
  • Beaumont Hospital
  • New York University Hospital
  • Stony Brook University Hospital
  • Wake Forest University Health Systems
  • Hillcrest Hospital
  • Cleveland Clinic Foundation
  • The Ohio State University Heart Center
  • Oklahoma University Health Sciences Center
  • Hospital of the University of Pennsylvania
  • Medical University of South Carolina
  • Texas Cardiac Arrhythmia Research
  • University of Texas, Southwestern
  • University of Virginia
  • Sentara Norfolk General Hospital
  • Homolka Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control

Treatment

Arm Description

Class I or III anti-arrhythmic drug for the treatment of AF

Pulmonary vein ablation with HIFU

Outcomes

Primary Outcome Measures

Acute treatment with elimination of AF episodes
Death, stroke, and hospitalization for recurrence of AF

Secondary Outcome Measures

Acute treatment success

Full Information

First Posted
October 24, 2006
Last Updated
June 16, 2008
Sponsor
ProRhythm, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00392106
Brief Title
High Intensity Focused Ultrasound (HIFU) Ablation System Study
Official Title
Study of Focused Circumferential UltraSound for the Treatment of Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Suspended
Why Stopped
voluntarily by Sponsor to investigate an anticipated SAE
Study Start Date
April 2006 (undefined)
Primary Completion Date
December 2010 (Anticipated)
Study Completion Date
June 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
ProRhythm, Inc.

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine if the HIFU Pulmonary Vein Ablation System is effective in the treatment of paroxysmal Atrial Fibrillation compared to the control of best medical therapy with FDA approved antiarrhythmic drugs.
Detailed Description
Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia affecting an estimated 2.2 million persons in the United States (US). In addition to being debilitating, AF has been identified as a leading risk factor for stroke. AF is often associated with structural heart disease, but a substantial number of AF patients have little or no detectable structural heart disease. A patient with AF is up to 5 times more likely to have a stroke than the general population. Recently, it has been demonstrated that for a significant portion of AF patients (80% - 95 %) the arrhythmia originates in one of the four pulmonary veins (PV's). Furthermore, it has been shown that isolation of this arrhythmia by ablation can, in the majority of patients (50-70%), eliminate or markedly reduce episodes of AF. Currently, there are a number of modalities being investigated to treat AF. They include radiofrequency, laser, thermal, cryo, microwave, and ultrasound ablation of targeted areas in the atrium and/or PVs. Comparison(s): Clinical success of High Intensity Focused Ultrasound (HIFU) Ablation for Pulmonary Vein Isolation in the treatment of Atrial Fibrillation, compared to medical therapy with anti-arrhythmic drugs (AADs).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
atrial fibrillation, arrhythmia, AF ablation, antiarrhythmic agent, catheter ablation, pulmonary veins

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
Class I or III anti-arrhythmic drug for the treatment of AF
Arm Title
Treatment
Arm Type
Experimental
Arm Description
Pulmonary vein ablation with HIFU
Intervention Type
Drug
Intervention Name(s)
propafenone
Other Intervention Name(s)
Rhyhmol
Intervention Description
Anti-arrhythmic drug prescribed for treatment of atrial fibrillation
Intervention Type
Drug
Intervention Name(s)
flecainide
Other Intervention Name(s)
Tambocor
Intervention Description
Anti-arrhythmic drug prescribed for the treatment of Atrial fibrillation
Intervention Type
Drug
Intervention Name(s)
dofetilide
Other Intervention Name(s)
Tikosyn
Intervention Description
Anti-arrhythmic drug prescribed for treatment of atrial fibrillation
Intervention Type
Drug
Intervention Name(s)
sotolol
Other Intervention Name(s)
Betapace
Intervention Description
Anti-arrhythmic Drug prescribed for treatment of Atrial Fibrillation
Intervention Type
Device
Intervention Name(s)
Pulmonary vein ablation
Other Intervention Name(s)
Left atrial ablation
Intervention Description
Electrical isolation of pulmonary vein with high-intensity focused ultrasound
Intervention Type
Drug
Intervention Name(s)
Amiodarone
Other Intervention Name(s)
Pacerone
Intervention Description
Anti-arrhythmic Drug prescribed for the treatment of Atrial Fibrillation
Primary Outcome Measure Information:
Title
Acute treatment with elimination of AF episodes
Time Frame
12 months
Title
Death, stroke, and hospitalization for recurrence of AF
Time Frame
within 12 months of treatment
Secondary Outcome Measure Information:
Title
Acute treatment success
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Documented atrial fibrillation Failed or intolerant to at least 1 anti-arrhythmic drug Able to take anti-coagulant therapy Able to complete screening tests required for inclusion/exclusion criteria Able to take at least 1 approved anti-arrhythmic drug Not pregnant Available for follow-up for at least 12 months Exclusion Criteria: Persistent or permanent atrial fibrillation Mitral disease Prior surgical treatment for atrial fibrillation Ablation for treatment of atrial fibrillation within 6 months Severe left ventricular hypertrophy Known untreated coagulopathy Unstable angina Prior stroke Uncontrolled heart failure Secondary causes of atrial fibrillation Uncorrected hyperthyroidism within 12 months Pulmonary embolism within 6 months Pneumonia or acute pulmonary disease within 3 months Pacemaker/ICD High risk for esophageal disease Currently enrolled in investigational drug or device study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Warren Jackman, MD
Organizational Affiliation
Oklahoma University Health Sciences Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hugh Calkins, MD
Organizational Affiliation
Johns Hopkins Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fullerton Vascular Medical Group
City
Fullerton
State/Province
California
ZIP/Postal Code
92835
Country
United States
Facility Name
University of California, Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
Piedmont Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30309
Country
United States
Facility Name
Lexington Central Baptist Hospital
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40503
Country
United States
Facility Name
Johns Hopkins Hopsital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
Lahey Clinic
City
Burlington
State/Province
Massachusetts
ZIP/Postal Code
01805
Country
United States
Facility Name
Beaumont Hospital
City
Royal Oak
State/Province
Michigan
ZIP/Postal Code
48220
Country
United States
Facility Name
New York University Hospital
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Stony Brook University Hospital
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794
Country
United States
Facility Name
Wake Forest University Health Systems
City
Winston Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Facility Name
Hillcrest Hospital
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44124
Country
United States
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
The Ohio State University Heart Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Oklahoma University Health Sciences Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
Facility Name
Texas Cardiac Arrhythmia Research
City
Austin
State/Province
Texas
ZIP/Postal Code
78705
Country
United States
Facility Name
University of Texas, Southwestern
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States
Facility Name
Sentara Norfolk General Hospital
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
Facility Name
Homolka Hospital
City
Prague
Country
Czech Republic

12. IPD Sharing Statement

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High Intensity Focused Ultrasound (HIFU) Ablation System Study

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