SPARK: Safety Study of Pradaxa in Atrial Fibrillation Patients by Regulatory Requirement of Korea
NCT01774370 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3182
Last updated 2019-03-08
Summary
This is a prospective, non-interventional, open-label, multi-centre study. It will provide additional safety information of Pradaxa in Korean patients with non-valvular AF in clinical settings.
Conditions
Interventions
- DRUG
-
Pradaxa (Dabigatran etexilate mesilate)
110 mg or 150 mg b.i.d.
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Boehringer Ingelheim · Boehringer Ingelheim
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-01-14
- Primary Completion
- 2017-02-17
- Completion
- 2017-02-17
Countries
- South Korea
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