Study to Test the Accuracy of a Prototype Handheld PT/INR Device

NCT01349712 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2011-05-09

No results posted yet for this study

Summary

The purpose of this study is to measure prothrombin time (PT) on an experimental device and a commercially available device on persons receiving coumadin (warfarin)treatment.

Conditions

  • Blood Coagulation Disorders

Sponsors & Collaborators

  • Universal Biosensors Pty Ltd

    lead INDUSTRY

Principal Investigators

  • Richard Ward, Pharm D · Harding University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2011-11-30
Completion
2011-11-30

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 NCT01349712 on ClinicalTrials.gov