Your session is about to expire
← Back to Search
Other
2-HOBA for Atrial Fibrillation Recurrence
Phase 2
Waitlist Available
Led By Greg Michaud, MD
Research Sponsored by Vanderbilt University Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
First time AF ablation with radiofrequency or cryo ablation
22 years of age or older
Must not have
Amiodarone within past 3 months
Planned surgical or hybrid (surgical + catheter) ablation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post-ablation for 28 days
Summary
This trial is testing whether a new treatment can help patients with atrial fibrillation (AF) who are undergoing a heart procedure called ablation. The goal is to see if this treatment can prevent early recurrence of AF by neutralizing harmful substances released during the procedure. The study will use smartwatches to monitor heart activity and measure the effectiveness of the treatment.
Who is the study for?
This trial is for adults aged 22 or older who are undergoing their first catheter-based ablation for atrial fibrillation, or a repeat procedure if they have persistent AF. Participants must be able to consent in writing and not have used certain medications like amiodarone recently, nor should they have severe heart failure, kidney issues, life expectancy under one year, or be pregnant.
What is being tested?
The study tests whether taking the antioxidant compound 2-Hydroxybenzylamine (2-HOBA) before an ablation can prevent early recurrence of atrial fibrillation by reducing oxidative stress. Patients will either receive 2-HOBA or a placebo starting seven days before the procedure. The effectiveness will be monitored daily using smartwatch ECG recordings.
What are the potential side effects?
While specific side effects of 2-HOBA aren't detailed here, participants might experience typical reactions associated with supplements such as digestive discomfort. Any medication could potentially cause allergic reactions or interact with existing conditions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am having my first AF ablation using either radiofrequency or cryo.
Select...
I am 22 years old or older.
Select...
I need another AF ablation because my atrial fibrillation persists and the doctor plans to target areas outside the pulmonary veins.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have not taken Amiodarone in the last 3 months.
Select...
I am scheduled for a surgery that involves removing or destroying tissue.
Select...
I have severe heart failure.
Select...
I have a condition like rheumatoid arthritis or psoriasis.
Select...
I am currently taking oral steroids or colchicine.
Select...
I have not had heart or chest surgery in the last 6 months.
Select...
I have had or am planning to have a heart transplant.
Select...
I am currently taking MAO inhibitors.
Select...
I have active heart-related chest pain.
Select...
I have been diagnosed with Hypertrophic Cardiomyopathy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre-ablation.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-ablation.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
2-HOBA reduces the rate of early recurrence of AF, atrial tachycardia, or atrial flutter following AF ablation within 28 days follow-up
A secondary analysis will analyze a surrogate of AF burden as the endpoint and designed to account for the impact of cardioversion on AF burden assessment
Secondary study objectives
2-HOBA reduces the change in IsoLG-adduct levels that occurs with AF ablation.
Other study objectives
Atrial Fibrillation
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: 2-HOBAActive Control1 Intervention
2-Hydroxybenzylamine(2-HOBA) 250 mg three tabs TID (po) for seven days prior to ablation and 28 days post ablation.
Group II: PlaceboPlacebo Group1 Intervention
Placebo- three tabs TID (po) for seven days prior to ablation and 28 days post-ablation
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 anticoagulants, antiarrhythmic drugs, and catheter ablation. Anticoagulants, such as warfarin and direct oral anticoagulants (DOACs), prevent blood clots and reduce the risk of stroke by inhibiting clotting factors.
Antiarrhythmic drugs, like amiodarone and flecainide, work by stabilizing the electrical activity of the heart to maintain a regular rhythm. Catheter ablation targets and destroys small areas of heart tissue that cause irregular electrical signals.
The trial studying 2-HOBA focuses on preventing oxidative stress-related tissue injury by inactivating IsoLGs, which could reduce early recurrence of AF post-ablation. This is important for AF patients as it addresses a specific cause of AF recurrence, potentially improving long-term outcomes and reducing the need for repeated interventions.
Does prophylactic therapy with antioxidant vitamins have an effect on atrial fibrillation following cardiac surgery?
Does prophylactic therapy with antioxidant vitamins have an effect on atrial fibrillation following cardiac surgery?
Find a Location
Who is running the clinical trial?
American Heart AssociationOTHER
344 Previous Clinical Trials
4,971,306 Total Patients Enrolled
11 Trials studying Atrial Fibrillation
92,143 Patients Enrolled for Atrial Fibrillation
Vanderbilt University Medical CenterLead Sponsor
900 Previous Clinical Trials
939,407 Total Patients Enrolled
12 Trials studying Atrial Fibrillation
5,503 Patients Enrolled for Atrial Fibrillation
Greg Michaud, MDPrincipal InvestigatorVanderbilt University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have not taken Amiodarone in the last 3 months.I am scheduled for a surgery that involves removing or destroying tissue.I have severe heart failure.I have a condition like rheumatoid arthritis or psoriasis.Your heart's pumping function is less than 35%.I am having my first AF ablation using either radiofrequency or cryo.I am 22 years old or older.I need another AF ablation because my atrial fibrillation persists and the doctor plans to target areas outside the pulmonary veins.I am currently taking oral steroids or colchicine.Doctors think you may live for less than a year.Your kidneys are not working well enough (creatinine clearance less than 30 ml/min).I have not had heart or chest surgery in the last 6 months.I have had or am planning to have a heart transplant.I am currently taking MAO inhibitors.I have active heart-related chest pain.I have been diagnosed with Hypertrophic Cardiomyopathy.You are allergic to aspirin.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: 2-HOBA
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.
Atrial Fibrillation Patient Testimony for trial: Trial Name: NCT04433091 — Phase 2
Share this study with friends
Copy Link
Messenger