Reporting of Adverse Events in Patients Treated With New Oral Anticoagulants

NCT02107651 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2014-04-24

No results posted yet for this study

Summary

Serious adverse events in patients treated with new oral anticoagulants are underreported.

Conditions

  • Bleeding as Complication to Anticoagulation Therapy

Sponsors & Collaborators

  • Hvidovre University Hospital

    lead OTHER

Principal Investigators

  • Bisgaard Thue, Ph.D · Hvidovre University Hospital

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • Denmark

Study Locations

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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 NCT02107651 on ClinicalTrials.gov