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NOACs Use in AF or VTE (SUNSHINE Registry)

The outcomes regiStry for non-vitamin k antagonist oral anticoagUlants treatmeNt in variouS tHrombotIc dIseases for better cliNical practicE (SUNSHINE) is a multicenter, prospective, observational non-interventional inpatient/outpatient disease registry to assess the utilization of Non-vitamin k antagonist oral anticoa

Condition(s)Atrial Fibrillation, Venous Thromboembolism, Oral Anticoagulant
StatusRecruiting
Study typeObservational
SummaryThe outcomes regiStry for non-vitamin k antagonist oral anticoagUlants treatmeNt in variouS tHrombotIc dIseases for better cliNical practicE (SUNSHINE) is a multicenter, prospective, observational non-interventional inpatient/outpatient disease registry to assess the utilization of Non-vitamin k antagonist oral anticoagulants (NOACs), and associated outcomes. The SUNSHINE registry will focus on the collection and analysis of observational data in medical records from hospital information system (HIS) to evaluate the outcomes related with these NOACs when applied in extensive patient populations outside of clinical research studies. The registry will also allow for mainly combining the atrial fibrillation (AF) and venous thromboembolism (VTE) databases. In brief, the SUNSHINE registry will
Who can participateInclusion Criteria: * Patients with clinically diagnosed with AF (eg, by electrocardiogram, Holter monitoring, implanted device, etc) or VTE (initial or recurrent acute VTE) * Patients who use OACs therapy (including NOAC or VKA) within the preceding 3 months * Patients can be enrolled from both inpatient or outpatient settings Exclusion Criteria: * AF resulting from reversible cause factors (e.g., thyroid disease, postoperative AF) * Patients with a diagnosis of valvular AF (valvular AF mainly refers to patients with AF that have either rheumatic valvular disease \[predominantly mitral stenosis\] or mechanical heart valves) * Patients participating in an ongoing clinical trial in AF or VTE * Have Multiple anticoagulation indications apart from AF or VTE * Patients with incomplete informat
SexAll
Lead sponsorHenan Provincial People's Hospital
LocationsZhengzhou, Henan, China
Start date2022-06-06
NCT IDNCT05378308
Official listinghttps://clinicaltrials.gov/study/NCT05378308

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