Preventing Cardiotoxicity in Breast Cancer Patients: PROACT

  • Research type

    Research Study

  • Full title

    Preventing cardiac damage in patients treated for breast cancer: a phase 3 Randomised, Open label, blinded endpoint, trial of enalapril to prevent Anthracycline-induced CardioToxicity (PROACT).

  • IRAS ID

    213348

  • Contact name

    David Austin

  • Contact email

    David.Austin@stees.nhs.uk

  • Sponsor organisation

    South Tees Hospitals NHS Foundation Trust

  • Eudract number

    2017-001094-16

  • Duration of Study in the UK

    2 years, 5 months, 31 days

  • Research summary

    Breast cancer is the most common type of cancer amongst women worldwide, with over 50,000 new cases in the UK every year. Treatment often includes surgery, chemotherapy and radiotherapy and is highly effective.

    However, the chemotherapy commonly given is a type called anthracyclines, which can cause damage to the heart cells. This may in turn lead to poorer heart function and heart failure.

    In this study, we would like to understand if a commonly used heart drug called enalapril can stop patients who are receiving anthracycline-based chemotherapy for their breast cancer from getting heart damage.

  • REC name

    West Midlands - Edgbaston Research Ethics Committee

  • REC reference

    17/WM/0248

  • Date of REC Opinion

    8 Aug 2017

  • REC opinion

    Further Information Favourable Opinion