Evaluation of the Amigo Robotic System for Ablation of the Cavo-Tricuspid Isthmus (Amigo-AFL)
Primary Purpose
Atrial Fibrillation, Atrial Flutter
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Amigo™ Robotic Catheter Manipulation
Manual Catheter Manipulation
Sponsored by
About this trial
This is an interventional treatment trial for Atrial Fibrillation focused on measuring Arrhythmia, cavo-tricuspid isthmus, atrial fibrillation, atrial fibrillation ablation
Eligibility Criteria
Inclusion Criteria:
- Must be scheduled to undergo radiofrequency catheter ablation of the cavo-tricuspid isthmus for atrial fibrillation (AF) or atrial flutter (AFL) according to appropriate clinical indications.
- Must be able and willing to provide written informed consent
- Must be at least 18 years old.
Exclusion Criteria:
- Patient's refusal to participate in the study
- Lack of indication for CTI ablation (eg: prior CTI ablation with persistent bidirectional isthmus block)
- Pregnancy
Sites / Locations
- Sulpizio Cardiovascular Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Manual Catheter Manipulation
Amigo™ Robotic Catheter Manipulation
Arm Description
25 subjects will be randomized to this arm. Manual catheter ablation of the cavo-tricuspid isthmus will be performed.
25 subjects will be randomized to this arm. Robotic catheter ablation of the cavo-tricuspid isthmus with the Amigo Catheter System will be performed.
Outcomes
Primary Outcome Measures
Contact Force Through Measurement of Force-time Integral (FTI)
Determination of the average total contact force (measured in gs) achieved during each ablation lesion using the Carto Mapping System
Secondary Outcome Measures
Fluoroscopy Time Measurements
Determine fluoroscopy time to reach CTI block.
Full Information
NCT ID
NCT02467179
First Posted
June 3, 2015
Last Updated
June 7, 2019
Sponsor
University of California, San Diego
Collaborators
Catheter Robotics, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT02467179
Brief Title
Evaluation of the Amigo Robotic System for Ablation of the Cavo-Tricuspid Isthmus
Acronym
Amigo-AFL
Official Title
Evaluation of the Amigo Robotic System for Ablation of the Cavo-Tricuspid Isthmus
Study Type
Interventional
2. Study Status
Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
March 2015 (Actual)
Primary Completion Date
October 30, 2017 (Actual)
Study Completion Date
March 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
Catheter Robotics, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare standard manual and robotically controlled catheter ablation of the cavo-tricuspid isthmus (CTI) as a treatment for atrial flutter. Ablation of the CTI is standard treatment for patients with a history of atrial flutter, and those undergoing ablation for atrial fibrillation. Both manual and robotic catheter manipulation are used in standard clinical practice at The University of California, San Diego (UCSD) for ablation.
Detailed Description
Dr. Gregory Feld, M.D. is conducting a research study to find out more about the effects of using the Amigo™ Robotic System for ablation of the cavo-tricuspid isthmus (flutter isthmus) on catheter stability (stabilization of the catheter during the procedure in order to prevent movement and dislodgement) using a combination of contact force (a measurement of the force applied by the catheter tip against the tissue during the ablation procedure), location, and duration measurements during ablation of the atrial flutter circuit. Published studies have indicated that robotic catheter manipulation is safe, may reduce patient and physician x-ray exposure, and ablation procedure time. Measuring contact force has also been shown to improve both short-term and long-term procedure success. However, research on ablation of the CTI specifically, is limited. This is a randomized study comparing robotic catheter manipulation using the Amigo Robotic System to manual catheter manipulation for ablation of the CTI on measures including catheter stability, contact force, procedure time, and fluoroscopy (X-ray) time.
The ablation procedure is standard of care, however, if patients chose to enroll in the study they will be randomized to one of two groups: either manual or robotic catheter manipulation. Throughout the procedure, research personnel will collect information from the procedure including measurements of contact force, catheter stability, procedure duration, and fluoroscopy (X-ray) time. If, in addition to ablation of the cavo-tricuspid isthmus for atrial flutter, a patient is scheduled to undergo ablation of the left atrium for atrial fibrillation or left atrial flutter, this will be performed subsequently in a standard manner, and will not be considered part of the research. Ablation of the CTI generally takes 45-60 minutes regardless of the technique used for manipulation of the catheters.
The patient's participation in the study will only last one day, the length of study procedure. There is no follow up associated with this study. All subjects will received standard of care treatment following their ablation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Atrial Flutter
Keywords
Arrhythmia, cavo-tricuspid isthmus, atrial fibrillation, atrial fibrillation ablation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Manual Catheter Manipulation
Arm Type
Active Comparator
Arm Description
25 subjects will be randomized to this arm. Manual catheter ablation of the cavo-tricuspid isthmus will be performed.
Arm Title
Amigo™ Robotic Catheter Manipulation
Arm Type
Experimental
Arm Description
25 subjects will be randomized to this arm. Robotic catheter ablation of the cavo-tricuspid isthmus with the Amigo Catheter System will be performed.
Intervention Type
Device
Intervention Name(s)
Amigo™ Robotic Catheter Manipulation
Other Intervention Name(s)
cavo-tricuspid isthmus ablation, atrial flutter ablation, arrhythmia, radiofrequency catheter ablation
Intervention Description
Ablation is a standard procedure that patients may undergo for the atrial flutter.
In this study, this group will be assigned to robotic catheter manipulation.
Intervention Type
Device
Intervention Name(s)
Manual Catheter Manipulation
Other Intervention Name(s)
cavo-tricuspid isthmus ablation, atrial flutter ablation, arrhythmia, radiofrequency catheter ablation
Intervention Description
Ablation is a standard procedure that patients may undergo for the atrial flutter.
In this study, this group will be assigned to manual catheter manipulation.
Primary Outcome Measure Information:
Title
Contact Force Through Measurement of Force-time Integral (FTI)
Description
Determination of the average total contact force (measured in gs) achieved during each ablation lesion using the Carto Mapping System
Time Frame
At time of the ablation procedure, which typically lasts 30-60 minutes
Secondary Outcome Measure Information:
Title
Fluoroscopy Time Measurements
Description
Determine fluoroscopy time to reach CTI block.
Time Frame
at time of ablation procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Must be scheduled to undergo radiofrequency catheter ablation of the cavo-tricuspid isthmus for atrial fibrillation (AF) or atrial flutter (AFL) according to appropriate clinical indications.
Must be able and willing to provide written informed consent
Must be at least 18 years old.
Exclusion Criteria:
Patient's refusal to participate in the study
Lack of indication for CTI ablation (eg: prior CTI ablation with persistent bidirectional isthmus block)
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gregory Feld, MD
Organizational Affiliation
UC San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sulpizio Cardiovascular Center
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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Evaluation of the Amigo Robotic System for Ablation of the Cavo-Tricuspid Isthmus
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