Validation of CoaguChek XS Pro near patient testing device

  • Research type

    Research Study

  • Full title

    Validation of CoaguChek XS Pro near patient testing device to measure patient INR

  • IRAS ID

    229595

  • Contact name

    Martin Drury

  • Contact email

    Martin.Drury@pbh-tr.nhs.uk

  • Sponsor organisation

    North West Anglia NHS Foundation Trust

  • Duration of Study in the UK

    0 years, 1 months, 21 days

  • Research summary

    We are introducing CoaguChek XS Pro (Roche) near patient testing devices to Peterborough City Hospital to measure patient INR. INR is the International normalised ratio, an assay evaluating the extrinsic pathway of coagulation. Part of the process to ensure the CoaguChek XP Pro is as efficient as the main analysers, a duplicate test on patients taking warfarin is required, along with the standard of care sample required by the main analysers. Patients having venesection for INR would be identified by the Anti-Coagulant Co-ordinator. A small sample of forty patients will consent to providing an additional finger prick blood test at the bedside, as well as their standard of care sample for the main analysers. There is no obligation for Patients to take this extra test. The blood from the finger prick will be tested on the CoaguChek XP Pro and the results stored for later analysis against the standard main analyser results.

  • REC name

    South West - Cornwall & Plymouth Research Ethics Committee

  • REC reference

    17/SW/0196

  • Date of REC Opinion

    16 Aug 2017

  • REC opinion

    Favourable Opinion