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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 belowSelect...
I have episodes of irregular heartbeat.
Select...
I have episodes of irregular heartbeat.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been diagnosed with sick sinus syndrome.
Select...
I have had surgery to remove part of my vagus nerve.
Select...
I frequently faint due to sudden drops in my heart rate and blood pressure.
Select...
I have a serious heart valve problem.
Select...
I have severe heart failure.
Select...
I am on dialysis for end-stage kidney disease.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
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.
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
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have episodes of irregular heartbeat.I am on dialysis for end-stage kidney disease.I have a serious heart valve problem.I have been diagnosed with sick sinus syndrome.I frequently faint due to sudden drops in my heart rate and blood pressure.You have specific heart rhythm issues without a pacemaker or a certain type of heart block.I have had surgery to remove part of my vagus nerve.Your heart's pumping function is less than 40%.I have not had a stroke in the last 3 months.I have not had a heart attack or been hospitalized for heart failure in the last 3 months.I have severe heart failure.I have episodes of irregular heartbeat.
Research Study Groups:
This trial has the following groups:- Group 1: Inactive TENS Stimulation
- Group 2: Active TENS Stimulation
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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