At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Norepinephrine (drug), Balanced Crystalloid (other)
- How long the study runs
- Study runs about 60 months (dates as stated)
- About the drug or intervention
- Norepinephrine — drug: Norepinepherine should be prepared and delivered at a concentration of 16 micrograms/ml · Balanced Crystalloid — other: IV fluids administered as per standard care
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 1,006
- Started
- 2022-10-11
- Last checked
- 2026-02
Plain English Summary
What is this study?
- • Testing a new treatment for sepsis
- • Phase3 - 1,006 participants
- • Sepsis is a life-threatening reaction to an infection
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with sepsis
Where?
- • Aintree - Aintree University Hospital
- • Blackburn - Royal Blackburn Hospital
- • Bury - Fairfield General Hospital
- • Cambridge - Addenbrookes Hospital, Cambridge
- • +21 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
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.
More detail
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.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
Biomarkers mentioned
What the study is looking for
- ✓Age \>18 years
- ✓Clinically suspected or proven infection resulting in principal reason for acute illness
- ✓SBP \< 90 mmHg or MAP of \< 65 mmHg (within an hour of eligibility assessment)
- ✓Hospital presentation within last 12 hours
Who cannot take part
- ✗\>1500ml of intravenous fluid prior to screening
- ✗Clinically judged to require immediate surgery (within one hour of eligibility assessment)
- ✗Immediate (\< 1 hour) requirement for central venous access
- ✗Chronic kidney replacement therapy
- ✗Known allergy/adverse reaction to norepinephrine
See the full criteria
Where Is This Study? (25 UK sites)
Aintree University Hospital
Aintree, United Kingdom
Royal Blackburn Hospital
Blackburn, United Kingdom
Fairfield General Hospital
Bury, United Kingdom
Addenbrookes Hospital, Cambridge
Cambridge, United Kingdom
Royal Derby Hospital
Derby, United Kingdom
Royal Infirmary of Edinburgh
Edinburgh, United Kingdom
Victoria Hospital
Fife Keith, United Kingdom
Glasgow Royal Infirmary
Glasgow, United Kingdom
Queen Elizabeth University Hospital
Glasgow, United Kingdom
Hull Royal Infirmary
Hull, United Kingdom
Kettering General
Kettering, United Kingdom
University Hospital Crosshouse
Kilmarnock, United Kingdom
University Hospital Monklands
Lanark, United Kingdom
Leicester Royal Infirmary
Leicester, United Kingdom
Carolyn Maloney
uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351Royal Liverpool University Hospital
Liverpool, United Kingdom
Newham University Hospital
London, United Kingdom
Royal London Hospital
London, United Kingdom
St George's
London, United Kingdom
Tania West, R&D Governance & Clinical Trials Manager
tania.west@swlstg.nhs.uk020 3513 6420University Hospital Lewisham
London, United Kingdom
John Radcliffe Hospital
Oxford, United Kingdom
Royal Alexandra Hospital
Paisley, United Kingdom
Peterborough City Hospital
Peterborough, United Kingdom
Royal Berkshire Hospital
Reading, United Kingdom
Queens Hospital Barking
Romford, United Kingdom
Salford Royal
Salford, United Kingdom
How to Get in Touch
Hannah Greenwood
Sponsor contactCONTACT
Alasdair Corfield
Sponsor contactCONTACT
