EVIS

  • Research type

    Research Study

  • Full title

    Early vasopressors in Sepsis

  • IRAS ID

    307862

  • Contact name

    Pamela Sandu

  • Contact email

    Pamela.Sandu@ggc.scot.nhs.uk

  • Eudract number

    2021-006886-39

  • Clinicaltrials.gov Identifier

    NCT05179499

  • Clinicaltrials.gov Identifier

    N/A, N/A

  • Duration of Study in the UK

    3 years, 8 months, 30 days

  • Research summary

    Sepsis is a life-threatening reaction to an infection. It happens when the immune system overreacts to an infection and starts to damage the body’s tissues and organs.

    The aim of this research study is to compare the effectiveness of giving a vasopressor drug (norepinephrine) against a Balanced Crystalloid both of which are given via a drip in the arm. Vasopressors work by increasing the blood pressure which allows a better blood flow to internal organs. We plan to see which is better and to see if they have a role in improving a patient’s recovery time, reducing complications, the length of time they stay in hospital and longer term poor health.

    Based on research that has already been done, we believe treating patients with vasopressors when they arrive in the Emergency Department, may have potential advantages over the standard fluids used today. However, the evidence is not clear and that is why we are doing this research.

  • REC name

    Scotland A: Adults with Incapacity only

  • REC reference

    22/SS/0009

  • Date of REC Opinion

    25 Apr 2022

  • REC opinion

    Further Information Favourable Opinion