Clinical Performance of Investigational InRhythm PT/INR System in a Professional Use Setting
Withdrawn
- Conditions
- Blood Dyscrasia
- Registration Number
- NCT02586818
- Lead Sponsor
- Accriva Diagnostics
- Brief Summary
This study is designed to evaluate and verify the clinical accuracy of the InRhythm PT/INR system; a point-of-care, whole blood PT/INR measurement with a reference plasma based PT/INR using a laboratory reference instrument and reagent (Sysmex/lnnovin) calibrated to the WHO rTF09 reference standard.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of INR measurements 5 weeks
- Secondary Outcome Measures
Name Time Method