Real Evidence of Anticoagulation Treatment in Non-valvular Atrial Fibrillation in Germany, UK and France: REACT-AF2

NCT02488421 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 38122

Last updated 2016-12-20

No results posted yet for this study

Summary

The purpose of this study is to determine and compare the persistence rate of newly prescribed apixaban, rivaroxaban, dabigatran and VKAs in patients with NVAF.

Conditions

  • Non-valvular Atrial Fibrillation

Sponsors & Collaborators

  • IMS Health

    collaborator OTHER
  • OXON Epidemiology

    collaborator INDUSTRY
  • Bristol-Myers Squibb

    lead INDUSTRY

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2016-07-31
Completion
2016-07-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02488421 on ClinicalTrials.gov