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

Study results available
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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

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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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 NCT01774370 on ClinicalTrials.gov