Atrial Fibrillation Clinical Trials
65 studies are recruiting for atrial fibrillation in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
By city
Studies now recruiting
-
The Rhythm Evaluation for AntiCoagulaTion With Continuous Monitoring of Atrial Fibrillation
REACT-AF is a multicenter prospective, randomized, open-label, blinded endpoint (PROBE design), controlled trial comparing the current Standard Of Care (SOC) of continuous Direct Oral Anticoagulation (DOAC) use versus time-delimited (1 month) DOAC guided by an AF-sensing Smart Watch (AFSW) in parti…
- Stage
- Phase 3
- Ages
- 22 to 85
- Site
- Banner University, Phoenix, Arizona
- Locations
- 93 in total
- Run by
- Johns Hopkins University
-
A Study of VARIPULSE Pulsed Field Ablation (PFA) Catheter and FARAWAVE PFA Catheter in the Treatment of Participants With Persistent Atrial Fibrillation
The purpose of this study is to assess how safe VARIPULSE pulsed field ablation (PFA) catheter is and how well it works compared to food and drug administration (FDA) approved FARAWAVE PFA catheter in participants with symptomatic persistent atrial fibrillation (PsAF; continuous irregular, rapid he…
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Arrhythmia Research Group, Jonesboro, Arkansas
- Locations
- 20 in total
- Run by
- Biosense Webster, Inc.
-
A Study of VARIPULSE Catheter in Participants With Persistent Atrial Fibrillation Undergoing Pulmonary Vein and Superior Vena Cava Isolation
The purpose of this study is to assess how safe VARIPULSE catheter system is for treatment of a heart rhythm disease called persistent atrial fibrillation (PsAF) in participants who are having a catheter ablation procedure (treat heart rhythm disease). This includes isolation of pulmonary vein and …
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Grandview Medical Center, Birmingham, Alabama
- Locations
- 13 in total
- Run by
- Biosense Webster, Inc.
-
PULSED AF Post-Approval Study
PULSED AF PAS is a prospective, global, multi-center, non-randomized, observational trial. Subjects will be treated with the PulseSelect™ PFA System and followed through 36 months.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Piedmont Heart Institute, Atlanta, Georgia
- Locations
- 23 in total
- Run by
- Medtronic Cardiac Ablation Solutions
-
A Study to Investigate the Efficacy, Safety, Tolerability and Pharmacokinetics of PKN605 in Participants With Atrial Fibrillation
A randomized, placebo-controlled, participant-and investigator-blinded study to evaluate the efficacy in reducing atrial fibrillation burden as well as the safety, tolerability and pharmacokinetics of PKN605 in participants with atrial fibrillation
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Cardiology Associates of North MS, Tupelo, Mississippi
- Locations
- 40 in total
- Run by
- Novartis Pharmaceuticals
-
Globe Registry: Globe® Pulsed Field System Registry Study for Treating Patients With Symptomatic Atrial Fibrillation
This post-market registry is designed to collect real world data on the use of the Globe PF System for the treatment of atrial fibrillation (AF).
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Arrhythmia Research Group, Jonesboro, Arkansas
- Locations
- 2 in total
- Run by
- Kardium Inc.
-
Pericardiotomy in Cardiac Surgery
PRINCE is an international, multicentre, randomized controlled trial of posterior pericardiotomy in patients without a history of atrial fibrillation (AF) or flutter undergoing cardiac surgery.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Louisville, Louisville, Kentucky
- Locations
- 19 in total
- Run by
- Population Health Research Institute
-
Repeatable Evaluation of Functional Intra-procedural Signals for Effect in Pulsed Field Ablation REFINE-PFA
The study is a prospective, exploratory observational study with the ECGenius® System and the PFAnalyzer software module in PFA cases using the FaraPulse PFA system. The cohort will be patients with paroxysmal or persistent atrial fibrillation (AF) who undergo PVI using this system.
- Stage
- Not phased
- Ages
- 21 and older
- Site
- The Valley Hospital, Paramus, New Jersey
- Locations
- 2 in total
- Run by
- CathVision ApS
-
Tulane iPredict, Prevent Study to Evaluate the Progression of Atrial Myopathy.
To evaluate the progression of atrial myopathy through wearable devices and cardiac imaging.
- Stage
- Not phased
- Ages
- 18 to 79
- Site
- Tulane University School of Medicine, New Orleans, Louisiana
- Run by
- Tulane University School of Medicine
-
A Study to Test How Well BAY 3670549 Works and How Safe it is in Patients With Atrial Fibrillation
The main goal of this study is to find out how well BAY 3670549 works, how safe it is, how well people can tolerate it, and how the body handles the medicine. The study will compare BAY 3670549 to a placebo (a dummy treatment with no active medicine) in people with AF who need a treatment called el…
- Stage
- Phase 2
- Ages
- 18 to 85
- Site
- Henry Ford Hospital - Cardiology, Detroit, Michigan
- Locations
- 30 in total
- Run by
- Bayer
-
Renal Denervation + PVI vs PVI Alone for Persistent AF
Pulmonary vein isolation (PVI) is the cornerstone of ablation for atrial fibrillation (AF). Increased cardiac sympathetic stimulation can facilitate AF and reduction can be accomplished by renal artery denervation (RDN). The recently completed randomized trial, ERADICATE-AF, convincingly demonstrat…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Rochester, Short Hills, New Jersey
- Run by
- University of Rochester
-
ReVeRA-301: Etripamil in Atrial Fibrillation Phase 3
This is a multi-national, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of etripamil NS in patients with atrial fibrillation (AF). This study includes Screening Visit, Randomization Visit, a Treatment Period with scheduled Follow-up Visits (Monthly Follow-…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Interventional Cardiology Medical Group (West Hills, CA), West Hills, California
- Locations
- 15 in total
- Run by
- Milestone Pharmaceuticals Inc.
-
Volunteers to Investigate Best Results for Ablation and Novel Therapies for Atrial Fibrillation
VIBRANT-AF seeks to: * Identify clinically relevant predictors of effectiveness and complications of AF ablation procedures in a prospective, US-based, multi-center, real-world longitudinal study * Assess changes in modifiable lifestyle-related exposures influence the effectiveness of AF ablation *…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of California, San Francisco, San Francisco, California
- Run by
- University of California, San Francisco
-
A Study Assessing Long-Term Safety and Effectiveness in Treatment Management of Atrial Fibrillation With VARIPULSE Catheter System
The purpose of this study is to evaluate the long-term safety and effectiveness of the FDA approved VARIPULSE catheter system for pulmonary vein isolation (PVI) in the treatment of participants with symptomatic paroxysmal atrial fibrillation (PAF).
- Stage
- Not phased
- Ages
- 22 and older
- Site
- Phoenix Cardiovascular Research Group, Phoenix, Arizona
- Locations
- 23 in total
- Run by
- Biosense Webster, Inc.
-
Comparing Magnesium 2g Versus 4g Versus Placebo in the Incidence of Treating AFF RVR
The purpose of this prospective, randomized, double-blinded study is to further evaluate the safety and efficacy of varying doses of intravenous magnesium in the treatment of AFF RVR.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Advocate Christ Medical Center Emergency Department (ACMC ED), Oak Lawn, Illinois
- Run by
- Wake Forest University Health Sciences
-
Comparing the Safety and Efficacy of Apixaban and Rivaroxaban
* The trial will compare two anticoagulants ("blood thinners") that are currently used in the VA and are considered standard care to prevent strokes in patients with atrial fibrillation. The two most commonly-used anticoagulants will be compared: apixaban (Eliquis) and rivaroxaban (Xarelto). They a…
- Stage
- Phase 4
- Ages
- 22 and older
- Site
- Miami VA Healthcare System, Miami, FL, Miami, Florida
- Locations
- 9 in total
- Run by
- VA Office of Research and Development
-
The Fourth Left Atrial Appendage Occlusion Study
LAAOS-4 aims to determine if catheter-based endovascular left atrial appendage occlusion prevents ischemic stroke or systemic embolism in participants with atrial fibrillation, who remain at high risk of stroke, despite receiving ongoing treatment with oral anticoagulation.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Arrhythmia Research Group, Jonesboro, Arkansas
- Locations
- 150 in total
- Run by
- Hamilton Health Sciences Corporation
-
Post-ablation Alcohol Impacts Arrhythmia Recurrence, Quality of Life and Cognition in AF
Earlier studies have shown a dose-dependent relationship between alcohol intake and incident atrial fibrillation (AF) as well as a causal link with several risk factors for AF such as hypertension, obesity and sleep apnea. However, the effect of drinking (alcohol) on post-ablation outcome such as a…
- Stage
- Not phased
- Ages
- 18 to 85
- Site
- Texas Cardiac Arrhythmia Institute, St. David's Medical Center, Austin, Texas
- Run by
- Texas Cardiac Arrhythmia Research Foundation
-
High-resolution MRI of Atrial Fibrillation Patients Prior to Focal Impulse and Rotor Modulation (FIRM) Ablation
Patients undergoing FIRM guided ablation of atrial fibrillation will undergo high resolution MRI imaging to determine correlation of underlying anatomic fibrotic regions with FIRM targeted sites for ablation.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Ohio State University, Columbus, Ohio
- Run by
- Ohio State University
-
CellFX® Nanosecond Pulsed Field Ablation (nsPFA)™ Cardiac Surgery Clamp System to Treat Atrial Fibrillation
The primary objective of this Pivotal study is to demonstrate the safety and effectiveness of the Pulse Biosciences nsPFA™ Cardiac Surgery System in treating atrial fibrillation during concomitant cardiac surgical procedures.
- Stage
- Not phased
- Ages
- 18 to 85
- Site
- Adventist Heart Institute: Adventist Health St. Helena, St. Helena, California
- Locations
- 3 in total
- Run by
- Pulse Biosciences, Inc.
-
Surveillance Trial of the Apple Watch in Reliable Burden Assessment in Unseen Recurrence of Surgically Treated AF
This is a prospective multicenter clinical study comparing the efficacy of the Apple Watch AFib History tool to the iRhythm Zio Patch monitoring device in quantifying atrial fibrillation (AF) burden after surgical ablation. Patients with AF and mitral valve (MV) disease who undergo a Cox-Maze IV pr…
- Stage
- Not phased
- Ages
- 22 and older
- Site
- Washington University School of Medicine in St. Louis, St Louis, Missouri
- Locations
- 2 in total
- Run by
- The Cleveland Clinic
-
Evaluation of 4D Intracardiac Echocardiography (ICE) During Structural Heart and Electrophysiology Procedures
The purpose of this study is to evaluate the imaging performance and procedural safety of a prototype 4D ICE catheter during real-time intracardiac imaging and to optimize device imaging parameters, compared with current standard imaging modalities. TEE is the current standard of care and will serv…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Cleveland Clinical Foundation, Cleveland, Ohio
- Run by
- The Cleveland Clinic
-
Exercise Activity Intervention With Sensor-Based Engagement in Patients With Atrial Fibrillation
Atrial fibrillation (AF) affects 1 in 4 individuals during their lifetime and continues to increase in frequency and impact. Exercise intervention has established benefits to improve AF symptoms and burden in clinical studies. However, lack of access to exercise programs has limited therapeutic ado…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Run by
- Icahn School of Medicine at Mount Sinai
-
NOrthwestern Tempus AI-enaBLed Electrocardiography (NOTABLE) Trial
The goal of this clinical trial is to determine if a machine learning/artificial intelligence (AI)-based electrocardiogram (ECG) algorithm (rECHOmmend and ECG-AF) can identify undiagnosed cardiovascular disease in patients. It will also examine the safety and effectiveness of using this AI-based to…
- Stage
- Not phased
- Ages
- 40 and older
- Site
- Northwestern University, Chicago, Illinois
- Run by
- Northwestern University
-
Carotid Implants for PreveNtion of STrokE ReCurrEnce From Large Vessel Occlusion in Atrial Fibrillation Patients Treated With Oral Anticoagulation
Patients with atrial fibrillation (AF) who have had a prior stroke are at very high risk of recurrent ischemic stroke. About 40% of these strokes are due to large emboli which result in large cerebral vessel occlusion (LVO). This randomized control trial aims to address this unmet need by testing w…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mercyhealth Javon Bea Hospital - Riverside, Rockford, Illinois
- Locations
- 21 in total
- Run by
- Javelin Medical
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.