Rivaroxaban Evaluation in Real Life Settings

NCT02444221 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5278

Last updated 2021-05-07

No results posted yet for this study

Summary

To discover outcomes of patients treated with Rivaroxaban with atrial fibrillation with at least one additional investigator-determined risk factor for stroke in real-life practice.

Conditions

Sponsors & Collaborators

  • Bayer

    collaborator INDUSTRY
  • Thrombosis Research Institute

    lead OTHER

Principal Investigators

  • Ajay Kakkar · Thrombosis Research Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-01
Primary Completion
2019-05-30
Completion
2020-09-30

Countries

  • France
  • United Kingdom

Study Locations

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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 NCT02444221 on ClinicalTrials.gov