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Ablation Device
Intramural Needle Ablation Catheter for Ventricular Tachycardia
N/A
Waitlist Available
Led By Usha Tedrow, M.D.
Research Sponsored by William Stevenson
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This study is evaluating whether a new device called an Intramural Needle Ablation Catheter (INA catheter) can help people who have ventricular arrhythmias that have failed standard radiofrequency ablation.
Eligible Conditions
- Ventricular Tachycardia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants With No Serious Adverse Events
Number of Subjects Ablated for Nonsustained Arrhythmias Who Had a Reduction to Less Than 5000 Arrhythmia Beats Daily
Number of Subjects Without Hospitalization for Ventricular Tachycardia (VT) During 6 Months
Secondary outcome measures
Number of Subjects With Acute Abolition of at Least One Clinical Inducible Ventricular Tachycardia or Targeted Nonsustained Arrhythmia
Trial Design
1Treatment groups
Experimental Treatment
Group I: Intramural Needle Catheter AblationExperimental Treatment1 Intervention
Ablation of Ventricular Tachycardia with Intramural Needle Ablation Catheter
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Intramural Needle Ablation Catheter
2016
N/A
~120
Find a Location
Who is running the clinical trial?
William StevensonLead Sponsor
William G. Stevenson, M.D.Study DirectorVanderbilt Heart and Vascular Institute
Usha Tedrow, M.D.Principal InvestigatorBrigham and Women's Hospital
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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