Atrial Fibrillation Clinical Trials in Washington D.C., District of Columbia
5 studies are recruiting for atrial fibrillation in Washington D.C., District of Columbia 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
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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
- St. Elizabeth's Medical Center, Washington D.C., District of Columbia
- Locations
- 93 in total
- Run by
- Johns Hopkins University
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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
- MedStar Washington Hospital, Washington D.C., District of Columbia
- Locations
- 29 in total
- Run by
- AtriCure, Inc.
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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
- MedStar Washington Hospital Center, Washington D.C., District of Columbia
- Locations
- 106 in total
- Run by
- Icahn School of Medicine at Mount Sinai
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Left Atrial Appendage Occlusion Registry (LAAO Registry)
The Left Atrial Appendage Occlusion Registry (LAAO Registry™) is designed to assess the prevalence, demographics, management, and outcomes of patients undergoing percutaneous and epicardial based left atrial appendage occlusion procedures to reduce the risk of stroke. Patient-level data will be sub…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- American College of Cardiology/National Cardiovascular Data Registry (NCDR), Washington D.C., District of Columbia
- Run by
- American College of Cardiology
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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
- MedStar Georgetown University Hospital, Washington D.C., District of Columbia
- Locations
- 187 in total
- Run by
- Yale University
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.