Phase
Condition
Soft Tissue Infections
Treatment
Balanced Crystalloid
Norepinephrine
Clinical Study ID
Ages > 18 All Genders
Study Summary
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
Study Description
Connect with a study center
Aintree University Hospital
Aintree,
United KingdomSite Not Available
Aintree University Hospital
Aintree 2657621,
United KingdomActive - Recruiting
City Hospital
Birmingham,
United KingdomSite Not Available
Royal Blackburn Hospital
Blackburn,
United KingdomSite Not Available
Royal Blackburn Hospital
Blackburn 2655524,
United KingdomTerminated
Fairfield General Hospital
Bury,
United KingdomSite Not Available
Fairfield General Hospital
Bury 2654187,
United KingdomActive - Recruiting
Addenbrookes Hospital, Cambridge
Cambridge 2653941,
United KingdomActive - Recruiting
Royal Derby Hospital
Derby,
United KingdomSite Not Available
Royal Derby Hospital
Derby 2651347,
United KingdomActive - Recruiting
Royal Infirmary of Edinburgh
Edinburgh,
United KingdomSite Not Available
Royal Infirmary of Edinburgh
Edinburgh 2650225,
United KingdomActive - Recruiting
Victoria Hospital
Fife Keith,
United KingdomSite Not Available
Victoria Hospital
Fife Keith 2649471,
United KingdomActive - Recruiting
Glasgow Royal Infirmary
Glasgow,
United KingdomSite Not Available
Queen Elizabeth University Hospital
Glasgow,
United KingdomSite Not Available
Glasgow Royal Infirmary
Glasgow 2648579,
United KingdomActive - Recruiting
Queen Elizabeth University Hospital
Glasgow 2648579,
United KingdomActive - Recruiting
Hull Royal Infirmary
Hull,
United KingdomSite Not Available
Hull Royal Infirmary
Hull 2645425,
United KingdomActive - Recruiting
Kettering General
Kettering,
United KingdomSite Not Available
Kettering General
Kettering 2645753,
United KingdomActive - Recruiting
University Hospital Crosshouse
Kilmarnock,
United KingdomSite Not Available
University Hospital Crosshouse
Kilmarnock 2645605,
United KingdomTerminated
University Hospital Hairmyres
Lanark,
United KingdomSite Not Available
University Hospital Monklands
Lanark,
United KingdomSite Not Available
University Hospital Monklands
Lanark 2644976,
United KingdomActive - Recruiting
Leicester Royal Infirmary
Leicester,
United KingdomSite Not Available
Leicester Royal Infirmary
Leicester 2644668,
United KingdomTerminated
Royal Liverpool University Hospital
Liverpool,
United KingdomSite Not Available
Royal Liverpool University Hospital
Liverpool 2644210,
United KingdomActive - Recruiting
Royal London Hospital
London,
United KingdomActive - Recruiting
St George's
London,
United KingdomActive - Recruiting
University Hospital Lewisham
London,
United KingdomSite Not Available
Newham University Hospital
London 2643743,
United KingdomActive - Recruiting
Royal London Hospital
London 2643743,
United KingdomActive - Recruiting
St George's
London 2643743,
United KingdomTerminated
University Hospital Lewisham
London 2643743,
United KingdomActive - Recruiting
John Radcliffe Hospital
Oxford,
United KingdomSite Not Available
John Radcliffe Hospital
Oxford 2640729,
United KingdomActive - Recruiting
Royal Alexandra Hospital
Paisley,
United KingdomSite Not Available
Royal Alexandra Hospital
Paisley 2640677,
United KingdomActive - Recruiting
Peterborough City Hospital
Peterborough,
United KingdomSite Not Available
Peterborough City Hospital
Peterborough 2640354,
United KingdomActive - Recruiting
Royal Berkshire Hospital
Reading,
United KingdomSite Not Available
Royal Berkshire Hospital
Reading 2639577,
United KingdomActive - Recruiting
Queens Hospital Barking
Romford,
United KingdomSite Not Available
Queens Hospital Barking
Romford 2639192,
United KingdomActive - Recruiting
Salford Royal
Salford,
United KingdomSite Not Available
Salford Royal
Salford 2638671,
United KingdomActive - Recruiting
Sandwell Hospital
West Bromwich,
United KingdomSite Not Available

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