RADAR Clinical Trial

Completed · Not applicable

Conditions studied: Persistent Atrial Fibrillation

In brief

This prospective, multicenter, observational study will examine the ability of real time electrogram processing mapping to identify driver domains to target for ablation in persistent AF patients.

Key facts

Study ID

NCT03263702

Run by

Vivek Reddy

People needed

65

Starts

2017-06-26

Expected to finish

2019-06-07

Last updated by the study team

2020-05-13

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ≥ 18 years of age.
• Patients are considered eligible if they have symptomatic or drug-refractory AF and are planned to undergo a catheter ablation procedure for persistent AF (ether a first procedure or a redo procedure)
• Ability to understand the requirements of the study and sign the informed consent form.
• Willingness to adhere to study restrictions and comply with all post-procedural follow-up requirements
• Projected lifespan greater than 1 year.

You may not qualify if…

• They have long-standing persistent AF prior to the first procedure (defined as AF greater than one year's duration).
• Rheumatic heart disease
• Current intra-cardiac thrombus
• History of MI or Coronary Artery Bypass Grafting (CABG) within 6 weeks
• Unstable angina
• CVA or TIA within 3 months
• Contraindication to anticoagulation
• Class IV HF
• Unable to sign consent
• Projected lifespan of < 1 year
• Women known to be pregnant or to have positive beta-HCG (Human Chorionic Gonadotropin).
• Participation in another study that would interfere with this study.

Where it is running

• University of Colorado Medical Center — Denver, Colorado, United States
• South Denver Cardiology — Denver, Colorado, United States
• Massachusetts General Hospital — Boston, Massachusetts, United States
• Icahn School of Medicine at Mount Sinai — New York, New York, United States

Full record on ClinicalTrials.gov

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