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Anticoagulation for Stroke Prevention In Patients With Recent Episodes of Atrial Fibrillation Occurring Transiently With Stress
NCT03968393 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Non-vitamin K oral anticoagulant (NOAC)
Study Locations (20)
New South Wales
- Bankstown Hospital — Bankstown
- Royal Prince Alfred Hospital — Camperdown
- Concord Repatriation General Hospital — Concord
- Liverpool Hospital — Liverpool
- John Hunter Hospital — Newcastle
- Westmead Hospital — Westmead
Other
- Hospital Municipal Chivilcoy — Chivilcoy
- Sanatorio Cisma — San Miguel de Tucumán
- Hospital Privado de Rosario — Santa Fe
Queensland
- Sunshine Coast Hospital and Health Service — Birtinya
- Royal Brisbane and Women's Hospital — Herston
- Redcliffe Hospital — Redcliffe
Santa Fe Province
- Instituto de Investigaciones Clinicas Rosario — Rosario
- Instituto Cardiovascular de Rosario — Rosario
California
- Cedars-Sinai Medical Center — Los Angeles
Texas
- Mcgovern Medical School at University of Texas — Houston
Buenos Aires
- Clinica Coronel Suarez — Coronel Suárez
Tucumán Province
- Centro Integral de Arritmias de Tucuman (CIAT) — San Miguel de Tucumán
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,270 participants |
| Start Date | 2019-06-14 |
| Est. Completion | 2028-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03968393
The ClinicalTrials.gov registry entry for NCT03968393 describes a study currently listed as recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Population Health Research Institute, which has 68 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Stroke appearing as the primary indexed condition, and to 1 intervention — of which Non-vitamin K oral anticoagulant (NOAC) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03968393 reports 20 study locations spanning 10 distinct geographic areas — top geographies include New South Wales, Other, Queensland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03968393 about?
NCT03968393 is a clinical study titled "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.
What is the current status of trial NCT03968393?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 2,270 participants. The study started on 2019-06-14. Estimated completion is 2028-12.
What conditions does trial NCT03968393 study?
This clinical trial studies the following conditions: Stroke, Atrial Fibrillation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03968393?
The interventions under investigation include: Non-vitamin K oral anticoagulant (NOAC) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03968393?
This trial is sponsored by Population Health Research Institute, which has 68 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03968393 being conducted?
This trial has 20 study locations across California, Texas, Buenos Aires, Santa Fe Province, Tucumán Province. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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