Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsPhase3

Early Vasopressors in Sepsis

Sponsor: NHS Greater Glasgow and Clyde

NCT ID: NCT05179499

View on ClinicalTrials.gov ↗

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.

Sepsis

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

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

have a negative

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
Inclusion Criteria: * 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) * Measured serum lactate of \> 2 mmol/L. The serum lactate should be measured 2 hours prior to determination of eligibility, where possible. Longer timeframes may be used and justified within the medical notes if, in the opinion of the investigator, the clinical status of the patient has not significantly improved in the time interval between lactate measurement and eligibility assessment. Lactate measurements more than 4 hours prior to eligibility assessment should not normally be used. * Hospital presentation within last 12 hours Exclusion Criteria: * \>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 renal replacement therapy * Known allergy/adverse reaction to norepinephrine * Palliation / end of life care (explicit decision by patient/family/carer in conjunction with clinical team that active treatment beyond symptomatic relief is not appropriate) * Previous recruitment in the trial * Patients with permanent incapacity * Pregnancy. All women of childbearing potential (WoCBP) must have a negative urine or serum 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 condition that would expose the subject to an undue risk of a significant Adverse Effect as determined by the clinical judgement of the investigator * Participation in other clinical trials of investigational medicinal products

Where Is This Study? (25 UK sites)

Aintree University Hospital

Aintree, United Kingdom

Recruiting
Site contact (verified)
Ben MortonPrincipal Investigator

Royal Blackburn Hospital

Blackburn, United Kingdom

TERMINATED

Fairfield General Hospital

Bury, United Kingdom

Recruiting
Site contact (verified)
Scott HoustonPrincipal Investigator

Addenbrookes Hospital, Cambridge

Cambridge, United Kingdom

Recruiting
Site contact (verified)
David LevertonPrincipal Investigator

Royal Derby Hospital

Derby, United Kingdom

Recruiting
Site contact (verified)
Andrew TabnerPrincipal Investigator

Royal Infirmary of Edinburgh

Edinburgh, United Kingdom

Recruiting
Site contact (verified)
Alasdair GrayPrincipal Investigator

Victoria Hospital

Fife Keith, United Kingdom

Recruiting
Site contact (verified)
Rajendra RamanPrincipal Investigator

Glasgow Royal Infirmary

Glasgow, United Kingdom

Recruiting
Site contact (verified)
Donogh MaguirePrincipal Investigator

Queen Elizabeth University Hospital

Glasgow, United Kingdom

Recruiting
Site contact (verified)
David LowePrincipal Investigator

Hull Royal Infirmary

Hull, United Kingdom

Recruiting
Site contact (verified)
Jack PreecePrincipal Investigator

Kettering General

Kettering, United Kingdom

Recruiting
Site contact (verified)
Maria iliescuPrincipal Investigator

University Hospital Crosshouse

Kilmarnock, United Kingdom

TERMINATED

University Hospital Monklands

Lanark, United Kingdom

Recruiting
Site contact (verified)
Nicola MoultriePrincipal Investigator

Leicester Royal Infirmary

Leicester, United Kingdom

TERMINATED
Hospital R&D contact (matched)

Carolyn Maloney

uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351

Royal Liverpool University Hospital

Liverpool, United Kingdom

Recruiting
Site contact (verified)
Ned Gilbert-KawaiPrincipal Investigator

Newham University Hospital

London, United Kingdom

Recruiting
Site contact (verified)
Ben BloomPrincipal Investigator

Royal London Hospital

London, United Kingdom

Recruiting
Site contact (verified)
Ben BloomPrincipal Investigator

St George's

London, United Kingdom

TERMINATED
Hospital R&D contact (matched)

Tania West, R&D Governance & Clinical Trials Manager

tania.west@swlstg.nhs.uk020 3513 6420

University Hospital Lewisham

London, United Kingdom

Recruiting
Site contact (verified)
anna colcloughPrincipal Investigator

John Radcliffe Hospital

Oxford, United Kingdom

Recruiting
Site contact (verified)
Deon LouwPrincipal Investigator

Royal Alexandra Hospital

Paisley, United Kingdom

Recruiting
Site contact (verified)
Santosh BongalePrincipal Investigator

Peterborough City Hospital

Peterborough, United Kingdom

Recruiting
Site contact (verified)
Christopher EdmundsPrincipal Investigator

Royal Berkshire Hospital

Reading, United Kingdom

Recruiting
Site contact (verified)
Matthew FrisePrincipal Investigator

Queens Hospital Barking

Romford, United Kingdom

Recruiting
Site contact (verified)
Darryl WoodPrincipal Investigator

Salford Royal

Salford, United Kingdom

Recruiting
Site contact (verified)
Daniel HornerPrincipal Investigator

How to Get in Touch

Hannah Greenwood

Sponsor contact

CONTACT

0141 314 4366 Hannah.Greenwood@nhs.scot

Alasdair Corfield

Sponsor contact

CONTACT

Alasdair.corfield2@nhs.scot
Data sourced from ClinicalTrials.gov · Last verified: 2026-02