Atrial Fibrillation Clinical Trials in Houston, Texas

6 studies are recruiting for atrial fibrillation in Houston, Texas 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.

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Studies now recruiting

  1. 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
    Baylor College of Medicine, Houston, Texas
    Locations
    93 in total
    Run by
    Johns Hopkins University
  2. Tracking Results of Ablations to Combat AF Registry Generation 2

    The primary objective of the TRAC-AF Registry is to capture real-world safety and effectiveness data on AtriCure devices used to conduct open concomitant and/or hybrid ablation, and management of the LAA concomitant to a cardiac ablation.

    Stage
    Not phased
    Ages
    18 and older
    Site
    Michael E. DeBakey VAMC - Houston, Houston, Texas
    Locations
    29 in total
    Run by
    AtriCure, Inc.
  3. Anticoagulation for New-Onset Post-Operative Atrial Fibrillation After CABG

    The primary objective of this study is to evaluate the effectiveness (prevention of thromboembolic events) and safety (major bleeding) of adding oral anticoagulation (OAC) to background antiplatelet therapy in patients who develop new-onset post-operative atrial fibrillation (POAF) after isolated c…

    Stage
    Phase 3
    Ages
    18 and older
    Site
    Baylor College of Medicine, Houston, Texas
    Locations
    106 in total
    Run by
    Icahn School of Medicine at Mount Sinai
  4. Anticoagulation in ICH Survivors for Stroke Prevention and Recovery

    Primary Aim: To determine if apixaban is superior to aspirin for prevention of the composite outcome of any stroke (hemorrhagic or ischemic) or death from any cause in patients with recent ICH and atrial fibrillation (AF). Secondary Aim: To determine if apixaban, compared with aspirin, results in b…

    Stage
    Phase 3
    Ages
    18 and older
    Site
    Houston Methodist Hospital, Houston, Texas
    Locations
    187 in total
    Run by
    Yale University
  5. Anticoagulation for Stroke Prevention In Patients With Recent Episodes of Atrial Fibrillation Occurring Transiently With Stress

    Multinational, investigator-initiated study of oral anticoagulation versus no anticoagulation for the prevention of stroke and other adverse cardiovascular events in patients with transient atrial fibrillation occurring transiently with stress and additional stroke risk factors.

    Stage
    Phase 4
    Ages
    55 and older
    Site
    Mcgovern Medical School at University of Texas, Houston, Texas
    Locations
    105 in total
    Run by
    Population Health Research Institute
  6. Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

    This study aims to identify genetic causes of adverse events after cardiac surgery, such as atrial fibrillation, myocardial infarction, renal dysfunction and heart failure. Patients undergoing heart surgery at Brigham and Women's Hospital and Texas Heart Institute are eligible to participate.

    Stage
    Not phased
    Ages
    20 to 90
    Site
    Department Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, Texas
    Locations
    3 in total
    Run by
    Brigham and Women's Hospital

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.