Actively Recruiting
Monitoring and Optimization of Cerebral Perfusion Pressure in Post-cardiac Arrest Patients: a Pilot Study
Led by National Taiwan University Hospital · Updated on 2024-12-16
50
Participants Needed
1
Research Sites
103 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this study is to establish the ICP and CPP monitoring process and analyze the results in post-arrest patients, to validate the correlation between direct and non-invasive ICP monitoring indicators, to establish a protocol of management of elevated ICP and insufficient CPP in post-arrest care, to establish a protocol for personalizing CPP and MAP optimization, and to analyze its impact on neuroprognosis. Participants will receive ICP monitoring within 12 hours post-ROSC if meet all inclusion and exclusion criteria.
CONDITIONS
Official Title
Monitoring and Optimization of Cerebral Perfusion Pressure in Post-cardiac Arrest Patients: a Pilot Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Non-traumatic cardiac arrest
- Admitted to intensive care unit (ICU)
- Glasgow Coma Scale motor score of 5 or less
- Medium-risk group according to TIMECARD severity score
You will not qualify if you...
- Traumatic cardiac arrest
- Pregnancy
- Intracranial hemorrhage
- Coagulopathy
- Use of anti-platelet or anti-coagulation medications
- Terminal illness
- Pre-arrest Cerebral Performance Category (CPC) score of 3 or higher
- Gray-White Matter Ratio (GWR) less than 1.2 on CT or severe hypoxic ischemic encephalopathy
- Central nervous system (CNS) infection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Taiwan University Hospital
Taipei, Taiwan
Actively Recruiting
Research Team
D
Dean-An Ling, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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