Early Vasopressors in Sepsis

Last updated: March 3, 2025
Sponsor: NHS Greater Glasgow and Clyde
Overall Status: Active - Recruiting

Phase

3

Condition

Soft Tissue Infections

Treatment

Balanced Crystalloid

Norepinephrine

Clinical Study ID

NCT05179499
GN20AE342
2021-006886-39
  • Ages > 18
  • All Genders

Study 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 two different ways to treat sepsis, in the early phase of treatment immediately after the participants arrive in hospital. The standard approach is to give a salt solution fluid through a drip in the participants arm to start with, then adding in a medication that increases the blood flow to the participants vital organs (a vasopressor mediation called norepinephrine) if required. The alternative approach is to start the vasopressor medication immediately, and then add in extra salt solution fluid via a drip if required. Vasopressors work by increasing the blood pressure which allows a better blood flow to the internal organs. The investigators plan to see which approach 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, the investigators 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 this research is being done.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age >18 years

  • Clinically suspected or proven infection resulting in principal reason for acuteillness

  • SBP < 90 mmHg or MAP of < 65 mmHg (within an hour of eligibility assessment)

  • Measured serum lactate of > 2 mmol/L. The serum lactate should be measured 2 hoursprior to determination of eligibility, where possible. Longer timeframes may be usedand justified within the medical notes if, in the opinion of the investigator, theclinical status of the patient has not significantly improved in the time intervalbetween lactate measurement and eligibility assessment. Lactate measurements morethan 4 hours prior to eligibility assessment should not normally be used.

  • Hospital presentation within last 12 hours

Exclusion

Exclusion Criteria:

  • >1500ml of intravenous fluid prior to screening

  • Clinically judged to require immediate surgery (within one hour of eligibilityassessment)

  • Immediate (< 1 hour) requirement for central venous access

  • Chronic renal replacement therapy

  • Known allergy/adverse reaction to norepinephrine

  • Palliation / end of life care (explicit decision by patient/family/carer inconjunction with clinical team that active treatment beyond symptomatic relief isnot appropriate)

  • Previous recruitment in the trial

  • Patients with permanent incapacity

  • Pregnancy. All women of childbearing potential (WoCBP) must have a negative urine orserum pregnancy test result completed as part of screening requirements.

WoCBP are defined as fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause.

  • Other primary causes of shock (e.g. suspected cardiogenic shock, haemorrhagic shock,etc)

  • History or evidence of any other medical, neurological or psychological conditionthat would expose the subject to an undue risk of a significant Adverse Effect asdetermined by the clinical judgement of the investigator

  • Participation in other clinical trials of investigational medicinal products

Study Design

Total Participants: 1005
Treatment Group(s): 2
Primary Treatment: Balanced Crystalloid
Phase: 3
Study Start date:
October 11, 2022
Estimated Completion Date:
October 31, 2027

Study Description

Sepsis results from overwhelming reactions to microbial infections where the immune system initiates dysregulated responses that lead to remote organ dysfunction, shock and ultimately death. Sepsis remains a significant global issue - as well as direct mortality, survivors suffer long term reductions in patient centred outcomes, with reduced quality of life and functional status. Patients with hypotension and organ hypoperfusion as a result of sepsis have poorer outcomes by dysregulated inflammation, endothelial dysfunction, immune suppression, and organ dysfunction. Current guidelines highlight the importance of early fluid resuscitation, but the association of early fluid therapy with improved outcomes is unclear. In the resuscitation phase, current practice is to give intravenous (IV) fluid and intermittent vasopressor boluses if required, before, for some patients, continuous vasopressor infusion via a central venous line in Intensive Care (ICU). An alternative, early continuous peripheral vasopressor infusion (PVI) is not routine practice in the UK.

Current practice in the UK is guided by NICE Sepsis guidance and the international Surviving Sepsis Campaign (SSC) consensus recommendations. Both specify intravenous fluid administration as a central tenet of early resuscitation of patients with septic shock, with intravenous vasopressor administration recommended after intravenous fluid resuscitation. NICE recommend boluses of 500ml of crystalloid and "refer to critical care for review of management including need for central venous access and initiation of vasopressors". SSC recommend 30ml/kg crystalloid in first hour, followed by vasopressors to maintain MAP>65.

The current NICE fluid resuscitation guideline, November 2020, continues to emphasise 500ml boluses of crystalloid as usual care. A recent international survey of 100 critical care and EM physicians regarding intravenous fluid resuscitation practice, confirmed that an initial bolus of 1000ml of crystalloid, followed by 500ml boluses of crystalloid remained the most common management strategy for the initial treatment of septic shock. This persisted despite the lack of benefit demonstrated in three landmark trials of protocolised sepsis management.

In recent years, there has been increasing acceptance of peripheral administration of norepinephrine, based on evidence of safety and efficacy. The Intensive Care Society published guidance on peripheral vasopressor infusion in November 2020. We have recently conducted a survey amongst ED and ICU clinicians in the UK regarding attitudes and current practice related to the use of intravenous peripheral vasopressors. Eighty two respondents provided the following answers

  1. Experience of use of any intravenous vasopressor in ED was high (81%);

  2. Exclusive PVI made up 23% of all vasopressor use in ED;

  3. Norepinephrine (norepinephrine) was the most common vasopressor (54%);

  4. Barriers to PVI were local protocols and an appropriate level of care in the destination ward for a patient on vasopressor infusion.

Connect with a study center

  • Aintree University Hospital

    Aintree,
    United Kingdom

    Site Not Available

  • City Hospital

    Birmingham,
    United Kingdom

    Site Not Available

  • Royal Blackburn Hospital

    Blackburn,
    United Kingdom

    Active - Recruiting

  • Fairfield General Hospital

    Bury,
    United Kingdom

    Site Not Available

  • Royal Derby Hospital

    Derby,
    United Kingdom

    Active - Recruiting

  • Royal Infirmary of Edinburgh

    Edinburgh,
    United Kingdom

    Active - Recruiting

  • Victoria Hospital

    Fife Keith,
    United Kingdom

    Active - Recruiting

  • Glasgow Royal Infirmary

    Glasgow,
    United Kingdom

    Site Not Available

  • Queen Elizabeth University Hospital

    Glasgow,
    United Kingdom

    Site Not Available

  • Hull Royal Infirmary

    Hull,
    United Kingdom

    Active - Recruiting

  • Kettering General

    Kettering,
    United Kingdom

    Active - Recruiting

  • University Hospital Crosshouse

    Kilmarnock,
    United Kingdom

    Site Not Available

  • University Hospital Hairmyres

    Lanark,
    United Kingdom

    Site Not Available

  • University Hospital Monklands

    Lanark,
    United Kingdom

    Active - Recruiting

  • Leicester Royal Infirmary

    Leicester,
    United Kingdom

    Site Not Available

  • Royal Liverpool University Hospital

    Liverpool,
    United Kingdom

    Site Not Available

  • Royal London Hospital

    London,
    United Kingdom

    Active - Recruiting

  • St George's

    London,
    United Kingdom

    Active - Recruiting

  • University Hospital Lewisham

    London,
    United Kingdom

    Site Not Available

  • John Radcliffe Hospital

    Oxford,
    United Kingdom

    Site Not Available

  • Royal Alexandra Hospital

    Paisley,
    United Kingdom

    Active - Recruiting

  • Peterborough City Hospital

    Peterborough,
    United Kingdom

    Active - Recruiting

  • Royal Berkshire Hospital

    Reading,
    United Kingdom

    Active - Recruiting

  • Queens Hospital Barking

    Romford,
    United Kingdom

    Site Not Available

  • Salford Royal

    Salford,
    United Kingdom

    Active - Recruiting

  • Sandwell Hospital

    West Bromwich,
    United Kingdom

    Site Not Available

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