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Neuromodulation Device

tVNS Device for Atrial Fibrillation

N/A
Recruiting
Led By Stavros Stavrakis, MD
Research Sponsored by University of Oklahoma
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
Must not have
Sick sinus syndrome
History of vagotomy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months

Summary

This trial tests if tVNS, which sends electrical pulses to the vagus nerve, can help patients with irregular heartbeats by regulating their heart rhythms. Vagus nerve stimulation has shown promise for managing heart rhythm issues.

Who is the study for?
This trial is for individuals with paroxysmal atrial fibrillation, which means their heart occasionally beats irregularly. It's not for those with significant heart valve issues, severe kidney disease on dialysis, pregnant women, certain types of heart block without a pacemaker, history of vagotomy or frequent fainting spells due to vasovagal syncope, very weak hearts (ejection fraction <40%), or recent stroke or serious heart events.
What is being tested?
The study tests if tVNS—a non-invasive nerve stimulation—can improve the condition and reduce episodes over six months compared to fake (sham) treatment. Researchers will also look for physical and biochemical signs that show who benefits most from this therapy.
What are the potential side effects?
While specific side effects are not listed here, transcutaneous electrical nerve stimulation devices like tVNS can sometimes cause skin irritation where they're applied and may lead to discomfort or tingling sensations during use.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have episodes of irregular heartbeat.
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I have episodes of irregular heartbeat.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have been diagnosed with sick sinus syndrome.
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I have had surgery to remove part of my vagus nerve.
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I frequently faint due to sudden drops in my heart rate and blood pressure.
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I have a serious heart valve problem.
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I have severe heart failure.
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I am on dialysis for end-stage kidney disease.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 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
Effects of tVNS on Atrial fibrillation burden
Secondary study objectives
Effects of tVNS on Autonomic Tone
Effects of tVNS on P wave alternans
Effects of tVNS on neuropeptide Y

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Active TENS StimulationActive Control1 Intervention
Group II: Inactive TENS StimulationPlacebo Group1 Intervention

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 rate control, rhythm control, and anticoagulation. Rate control medications, such as beta-blockers and calcium channel blockers, slow the heart rate by inhibiting the atrioventricular (AV) node. Rhythm control strategies, including antiarrhythmic drugs and cardioversion, aim to restore and maintain normal sinus rhythm. Anticoagulation therapy, using drugs like warfarin or direct oral anticoagulants, prevents thromboembolism, a major risk in AF patients. Treatments like transcutaneous Vagus Nerve Stimulation (tVNS) modulate the autonomic nervous system, potentially reducing AF episodes by enhancing parasympathetic activity and stabilizing heart rhythms. These mechanisms are crucial as they help manage symptoms, reduce stroke risk, and improve the quality of life for AF patients.
Neuromodulation for the Treatment of Heart Rhythm Disorders.

Find a Location

Who is running the clinical trial?

University of OklahomaLead Sponsor
473 Previous Clinical Trials
93,521 Total Patients Enrolled
13 Trials studying Atrial Fibrillation
2,448 Patients Enrolled for Atrial Fibrillation
Stavros Stavrakis, MDPrincipal InvestigatorUniversity of Oklahoma
6 Previous Clinical Trials
194 Total Patients Enrolled
3 Trials studying Atrial Fibrillation
63 Patients Enrolled for Atrial Fibrillation

Media Library

Transcutaneous Electrical Nerve Stimulation Device (Neuromodulation Device) Clinical Trial Eligibility Overview. Trial Name: NCT05172765 — N/A
Atrial Fibrillation Research Study Groups: Inactive TENS Stimulation, Active TENS Stimulation
Atrial Fibrillation Clinical Trial 2023: Transcutaneous Electrical Nerve Stimulation Device Highlights & Side Effects. Trial Name: NCT05172765 — N/A
Transcutaneous Electrical Nerve Stimulation Device (Neuromodulation Device) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05172765 — N/A
~48 spots leftby Oct 2025