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Patient Convenience Study (RE-SONANCE)

NCT02684981 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9472

Last updated 2019-07-24

Study results available
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Summary

The aim of this non-interventional study is to describe patient's perception of anticoagulant treatment when using Pradaxa to prevent stroke and systemic embolism while suffering from atrial fibrillation (according to its approved indication in the approved dosages of 110 milligrams or 150 milligrams twice daily) in comparison to standard care using Vitamin K Antagonist (VKA).

Conditions

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-11
Primary Completion
2017-06-01
Completion
2017-06-01

Countries

  • Austria
  • Bulgaria
  • Czechia
  • Estonia
  • Hungary
  • Israel
  • Latvia
  • Poland
  • Romania
  • Russia
  • Serbia
  • Slovenia

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Entities

Diseases
Companies

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 NCT02684981 on ClinicalTrials.gov