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Acute changes in metabolic parameters after bolus fluid treatment in critically ill patients

Completed
Conditions
Critically ill patients with suspected hypovolemia
Haematological Disorders
Hypovolemia
Registration Number
ISRCTN31590683
Lead Sponsor
CHU-Brugmann
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
100
Inclusion Criteria

1. Patient treated in ICU
2. Suspicion of hypovolemia that must be treated
3. Available central venous and arterial catheter
4. Available method for cardiac output measurment (thermodilution, doppler)

Exclusion Criteria

1. Aged under 18 year
2. No jugular or subclavian venous catheter and arterial catheter
3. Individuals on whom it is not possible to measure cardiac output
4. Patients receiving extracorporeal membrane oxygenation (ECMO) support
5. Receipt of interventions (i.e. introduction or increase in the dose of inotropes, changes or introduction of mechanical ventilation) within 30 minutes prior to fluid administration

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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