Determination of volume responsiveness in patients with acquired brain injury
Recruiting
- Conditions
- Patients with intracranial hemorrhage (spontaneous or traumatic)
- Registration Number
- DRKS00032021
- Lead Sponsor
- niversitätsklinikum Heidelberg, Klinik für Anästhesiologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Continuous ICP monitoring
Continuous blood pressure monitoring
Exclusion Criteria
Refusal by the patient or their caregiver
Absence of external ventricular drainage (EVD)/ICP probe
No arterial cannula for continuous blood pressure measurement
Pregnancy
Persistent pathologically elevated intracranial pressure
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in ICP and MAP values between baseline (before testing is performed) and the maximum or minimum value
- Secondary Outcome Measures
Name Time Method CPP, LVOT VTI, stroke volume, cardiac output and cardiac index