Actively Recruiting

All Genders
NCT05378308

NOACs Use in AF or VTE (SUNSHINE Registry)

Led by Henan Provincial People's Hospital · Updated on 2022-06-09

5000

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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 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 provide important information on the outcomes of NOACs in routine practice and gather further information on its safety and effectiveness.

CONDITIONS

Official Title

NOACs Use in AF or VTE (SUNSHINE Registry)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with clinically diagnosed atrial fibrillation or venous thromboembolism
  • Patients who have used oral anticoagulant therapy (NOAC or VKA) within the past 3 months
  • Patients can be enrolled from inpatient or outpatient settings
Not Eligible

You will not qualify if you...

  • Atrial fibrillation caused by reversible factors such as thyroid disease or postoperative AF
  • Diagnosis of valvular atrial fibrillation (including rheumatic valvular disease or mechanical heart valves)
  • Participation in an ongoing clinical trial for atrial fibrillation or venous thromboembolism
  • Having multiple anticoagulation indications other than atrial fibrillation or venous thromboembolism
  • Incomplete, illogical, or insufficient patient data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Henan Provincial People's Hospital

Zhengzhou, Henan, China, 450000

Actively Recruiting

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Research Team

S

Shujuan Zhao

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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