Low-Field Bedside Brain Magnetic Resonance Imaging in Pediatric Extracorporeal Membrane Oxygenation
NCT06074406
Acute Brain Injury, Brain Diseases
Kansas City, Missouri, United States
View Trial DetailsNCT Number: NCT00163800
This study will attempt to evaluate clinical, laboratory and radiographic parameters together to assess heir values in outcome prediction from brain injury. Patients will be followed up for a period of 6 months, following admission to ICU, to assess outcome, using the Extended Glasgow Outcome Score (GOSE).
We hypothesise that it is possible to reliably predict outcome in brain injury from the current investigations we have at our disposal.
Looking for future studies?
Notify Me16 year and older
All sexes
Observational
Design- A prospective clinical trial of patients admitted to intensive care with acute brain injury due to trauma.
Setting- Intensive Care Unit of the Alfred Hospital Clinical Examination- Day 4 and day 8, ICU consultant to assess prognosis and score patient.
Electrophysiology- Day 4 and day 8, SSEP and EEG. Interpretation by person blinded to the patient.
CT Brain- Day 1, day 4 and day 8. Interpretation by radiologist blinded to the patient.
Blinding- Persons blinded to the patients will make all interpretations of investigations. Mode of brain injury will be made available.
Follow up of patients- Structured interviews by telephone will be performed at 6 months post injury with the patient alone, relatives/ friend/ carer alone or patient and relatives/ friend/ carer. These will be performed in relation to the Extended Glasgow Outcome Scale (GOSE).
Statistics- The positive and negative predictive values for the tests will be determined.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Looking for future studies?
Notify MeBayside Health
Other Gov
Outcome Predictors in Acute Brain Injury, A Pilot Study
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