Microvisk Continuous Blood Donation Study

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMicrovisk Technologies Ltd

About this trial

Microvisk Technologies Ltd designs and develops test systems for monitoring the effectiveness of Warfarin and Warfarin-like medications.

Warfarin and Warfarin-like medications are used to reduce the risk of stroke in people with an irregular heart rhythm (Atrial Fibrillation) or with mechanical heart valve replacements, as well as reducing the risk of recurrent Venous Thromboembolism.

Warfarin dosing needs to be individualized. In order to correctly dose an individual in order to optimize the effectiveness of warfarin, and minimize the risk of bleeding, close monitoring of the degree of anticoagulation is required through regular blood testing. This test is known as PT/INR (Prothrombin Time/International Normalised Ratio). Simply, it is the measure of the amount of time (in seconds) it takes for your blood to clot.

Microvisk Technologies Ltd are developing new anticoagulant test strips for patients on warfarin or warfarin like medications. The blood collected as part of this study will be tested upon Microvisk's second generation Prothrombin/International Normalized Ratio (PT/INR) Test System. The donated blood will be used on ongoing development, validation, verification, and calibration projects. This study is being performed in partnership with the Oxford University Hospital (OUH) and Local Clinical Research Networks (LCRN) Thames Valley Core team, part of National Institute for Health and Care Research (NIHR).

Eligibility criteria

Qualifiers

Currently undergoing Warfarin therapy.

Over 18 years old

Disqualifiers

Participant is <18 years of age

Participant is unable to give consent

Participant has been treated with Unfractionated Heparin, or Low Molecular Weight Heparin, within the last 7 days

Participant has, or is suspected of having, Anti-Phospholipid Syndrome (APS)

Trial design

Treatments tested in this trial

  • Venepuncture
  • Collection of relevant information

Treatment groups

2,500 Participants
are divided into 1 treatment group

Sponsors and collaborators