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PT/INR Reference Interval IN Healthy Volunteers

NCT02319109 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 154

Last updated 2015-01-22

No results posted yet for this study

Summary

This is a prospective, single-center study in healthy volunteers to establish a PT/INR reference interval for the Microvisk International Normalized Ratio (INR) Test System. The primary objective of this study is to establish the reference interval for the measurement of prothrombin time (PT/INR) using the Microvisk INR Test System. The second objective is to evaluate the safety of the device.

Conditions

  • Healthy

Sponsors & Collaborators

  • Microvisk Technologies Ltd

    lead INDUSTRY

Principal Investigators

  • Helen Stacey, MD, PhD · Diablo Clinical Research

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2014-12-31
Completion
2015-01-31

Countries

  • United States

Study Locations

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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 NCT02319109 on ClinicalTrials.gov