Status:

COMPLETED

Post-Marketing Surveillance of Prazaxa® on the Long-term Use in Patients With Nonvalvular Atrial Fibrillation

Lead Sponsor:

Boehringer Ingelheim

Conditions:

Atrial Fibrillation

Eligibility:

All Genders

Brief Summary

To investigate the safety and efficacy of long-term use of Prazaxa® Capsules in patients with nonvalvular atrial fibrillation for preventing the occurrence of ischemic stroke or systemic embolism (SEE...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • \- Patients with nonvalvular atrial fibrillation who have never received Prazaxa Capsules for preventing the occurrence of ischemic stroke and systemic embolism will be included.
  • Exclusion criteria:
  • \- None

Exclusion

    Key Trial Info

    Start Date :

    December 12 2011

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    August 2 2016

    Estimated Enrollment :

    6772 Patients enrolled

    Trial Details

    Trial ID

    NCT01491178

    Start Date

    December 12 2011

    End Date

    August 2 2016

    Last Update

    January 30 2018

    Active Locations (1164)

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    Page 1 of 291 (1164 locations)

    1

    Boehringer Ingelheim Investigational Site 1

    Abashiri, Hokkaido, Japan

    2

    Boehringer Ingelheim Investigational Site 287

    Adachi,Tokyo, Japan

    3

    Boehringer Ingelheim Investigational Site 288

    Adachi,Tokyo, Japan

    4

    Boehringer Ingelheim Investigational Site 289

    Adachi,Tokyo, Japan

    Post-Marketing Surveillance of Prazaxa® on the Long-term Use in Patients With Nonvalvular Atrial Fibrillation | DecenTrialz