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Clinical Trial Summary

The investigators study aims to test the correlation between the Hemochron Signature point-of-care testing (POCT) device (ITC, USA) and low plasma levels of all three currently approved direct oral anticoagulants (DOAC; rivaroxaban, apixaban and dabigatran) and to determine the diagnostic accuracy of POCT to rule out or detect relevant levels of DOAC in real-life stroke patients.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Anticoagulation With Direct Oral Anticoagulants

NCT number NCT02371070
Study type Observational
Source University Hospital Tuebingen
Contact
Status Completed
Phase N/A
Start date December 2013
Completion date May 2016

See also
  Status Clinical Trial Phase
Completed NCT02371044 - Point-of-Care Testing of Coagulation in Patients Treated With Direct Oral Anticoagulants 1 N/A
Recruiting NCT04679298 - Point-of-Care Testing of Coagulation in Patients Treated With Direct Oral Anticoagulants Extended