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Antiarrhythmic

Radiofrequency Ablation vs Antiarrhythmic Drugs for Atrial Fibrillation (RAAFT-3 Trial)

Phase 3
Waitlist Available
Led By Andrea Natale, MD
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients symptomatic with persistent AF
Be older than 18 years old
Must not have
Absolute contra-indication to the use of heparin and/or oral anticoagulation
Women with a positive pregnancy test
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Awards & highlights
Pivotal Trial
No Placebo-Only Group

Summary

This trial is investigating whether a procedure called catheter ablation is better than medication for treating patients with persistent atrial fibrillation who haven't yet tried specific heart medications. Catheter ablation involves using a thin tube to create small scars in the heart, which helps stop irregular heartbeats. The goal is to see if this procedure can more effectively control symptoms and improve quality of life compared to starting with medication. Catheter ablation has been shown to be more effective than medication at restoring normal heart rhythm and improving quality of life in patients with atrial fibrillation.

Who is the study for?
This trial is for adults over 18 with persistent atrial fibrillation (AF), which means their heart has been in an irregular rhythm for more than 7 days. They must have had at least two AF episodes in the past 9 months, documented by ECG. People can't join if they have severe heart issues, previous AF treatments, are pregnant, or have conditions that could interfere with the study.
What is being tested?
The RAAFT-3 trial is testing whether using a procedure called Radio Frequency Catheter Ablation to isolate pulmonary veins works better as a first treatment for persistent AF compared to standard antiarrhythmic drugs.
What are the potential side effects?
Possible side effects from ablation include bleeding or bruising at the catheter site, damage to blood vessels or heart tissue, and risks associated with anesthesia. Antiarrhythmic drugs may cause nausea, dizziness, fatigue or more serious effects like organ dysfunction.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have ongoing symptoms from atrial fibrillation.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I cannot use heparin or blood thinners.
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I am currently pregnant.
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I have had a procedure to treat irregular heartbeat.
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I currently have a heart infection or a systemic infection.
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I have taken medication for irregular heartbeat before.
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I have severe heart artery blockage or had a recent heart bypass surgery.
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I do not have severe lung problems like COPD.
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I have a serious heart valve problem.
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I cannot have a catheter ablation due to a clot or abnormality in my heart's left atrium.
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I have a high risk of bleeding or a history of severe bleeding problems.
Select...
I cannot take any antiarrhythmic drugs like sotalol or amiodarone.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 18 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Recurrence of symptomatic Atrial Fibrillation
Secondary study objectives
AF/AT Burden
CV Hospitalizations
Quality of Life Questionnaire
+2 more

Awards & Highlights

Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Active Control
Group I: Antiarrhythmic MedicationsActive Control1 Intervention
Patients randomized to the antiarrhythmic drug group are administered medications approved for treatment of AF by the regulatory bodies of each participating country. The selection of antiarrhythmic drugs and dosages is left to the discretion of the investigator, and will follow the AHA/ACC/HRS general guidelines
Group II: Radio Frequency Catheter AblationActive Control1 Intervention
Patients randomized to radiofrequency catheter ablation will undergo isolation of the pulmonary veins with confirmation of entrance block into each vein. The CARTO TM(Biosense Webster, CA) system will be used to reconstruct the atrial geometry and assist for mapping and ablation. Ablation will be performed using approved ablation devices (Biosense Webster, CA).

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Atrial Fibrillation (AF) include rhythm control and rate control strategies. Rhythm control aims to restore and maintain a normal heart rhythm using antiarrhythmic drugs or catheter-based ablation, which disrupts abnormal electrical signals in the heart. Rate control focuses on controlling the heart rate with medications like beta blockers, calcium channel blockers, or digoxin. These treatments are important for AF patients as they help manage symptoms and reduce the risk of complications such as stroke.

Find a Location

Who is running the clinical trial?

University of PennsylvaniaLead Sponsor
2,072 Previous Clinical Trials
42,713,866 Total Patients Enrolled
16 Trials studying Atrial Fibrillation
2,475 Patients Enrolled for Atrial Fibrillation
Texas Cardiac Arrhythmia Research FoundationOTHER
38 Previous Clinical Trials
15,286 Total Patients Enrolled
27 Trials studying Atrial Fibrillation
8,551 Patients Enrolled for Atrial Fibrillation
Biosense Webster, Inc.Industry Sponsor
126 Previous Clinical Trials
37,074 Total Patients Enrolled
85 Trials studying Atrial Fibrillation
28,991 Patients Enrolled for Atrial Fibrillation

Media Library

Anti Arrhythmics (Antiarrhythmic) Clinical Trial Eligibility Overview. Trial Name: NCT04037397 — Phase 3
Atrial Fibrillation Research Study Groups: Antiarrhythmic Medications, Radio Frequency Catheter Ablation
Atrial Fibrillation Clinical Trial 2023: Anti Arrhythmics Highlights & Side Effects. Trial Name: NCT04037397 — Phase 3
Anti Arrhythmics (Antiarrhythmic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04037397 — Phase 3
Atrial Fibrillation Patient Testimony for trial: Trial Name: NCT04037397 — Phase 3
~20 spots leftby Nov 2025