The FORECAST Trial

  • Research type

    Research Study

  • Full title

    Fractional Flow Reserve Derived from Computed Tomography Coronary Angiography in the Assessment and Management of Stable Chest Pain.

  • IRAS ID

    231037

  • Contact name

    Nicholas Curzen

  • Contact email

    nick.curzen@uhs.nhs.uk

  • Sponsor organisation

    University Hospital Southampton NHS Foundation Trust

  • Clinicaltrials.gov Identifier

    NCT03187639

  • Duration of Study in the UK

    3 years, 0 months, 1 days

  • Research summary

    The best way to assess and manage patients presenting with stable chest pain likely to be angina is not clear. Tests that describe the size and shape of the arteries (anatomy) and how well the blood vessels are working (i.e. how easily the blood can flow through them, the physiology) are needed in order to work out the best treatment plan. Currently, patients may need to have more than one test to look at both the anatomy and the physiology. They may also be invasive and/or expensive (e.g. invasive coronary angiogram or a device known as a ‘pressure wire’).

    More recently pictures of the heart arteries have been taken using a CT (computerised tomography) heart scanner and a company called HeartFlow Inc®, has developed new software that allows a computer to generate information from a routine CT scan, called FFRct. This test can now give results about the size and shape (anatomy) of the blood vessels and can also calculate how well they function, by measuring the flow of blood going through the vessels (physiology), in a non-invasive way. This Trial will assess Standard investigations versus CT scan (with FFRct as required) within a randomised controlled trial.

    Patients who have been referred to a Rapid Access Chest Pain Clinic (RACPC) for investigation of their chest pain and are suitable for a CT scan, will be invited to participate. The study will take place in hospitals within the UK.

    Participants will be asked to sign consent form, complete questionnaires about their quality of life at the beginning of the study and will then either undergo standard investigations or CT scan (with FFR as required). They will then complete the same questionnaires, plus how satisfied they were with the treatment and what NHS resource they have used at 3 months and 9 months.

  • REC name

    South Central - Berkshire B Research Ethics Committee

  • REC reference

    17/SC/0490

  • Date of REC Opinion

    21 Sep 2017

  • REC opinion

    Favourable Opinion