Hypothermia Clinical Trial
In this pilot study the researchers will investigate efficacy of hypothermia in the early stage of treatment patients with primary intracerebral hemorrhage.
The purpose of this pilot trial is to determine whether hypothermia improves neurological
outcome (measured as 3 and 6 months after the onset of symptoms using mRS, GOS and BI) in
patients who has suffered a primary intracerebral hemorrhage. The patients with primary
intracerebral hemorrhage presented with coma (GCS ≤ 8) and ICH score 2-4 will be included.
Induction of hypothermia will be initiated within 6 hours of symptoms onset. Patients will
be cooled to core temperature of 34°C during 24 hours using non-invasive temperature
management (Cincinnati Sub-Zero). The temperature will be measured continuously by
esophageal system. After 24 hours of successful cooling, the target temperature will be
gradually raised to achieve slow re-warming of 0.5°C / 2 h until the core temperature
reaches 36,5°C.
During hypothermia ECG, blood pressure, oxygen saturation and intracranial pressure will be
measured continuously and registered every 30 min. The first CT scan of the brain, after
initial, will be done early after normothermia is reached.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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