Monitoring and Optimization of Cerebral Perfusion Pressure in Post-cardiac Arrest Patients: a Pilot Study
Recruiting
N/A
Interventional Study
Cardiac Arrest
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 50 (estimated)
- Sponsor
- National Taiwan University Hospital · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* non-traumatic cardiac arrest
* admitted to ICU
* GCS: motor \<=5
* severity: TIMECARD score medium-risk group
Exclusion Criteria:
* traumatic cardiac arrest
* pregnancy
* intracranial hemorrhage
* coagulopathy
* anti-platelet or anti-coagulation use
* terminal illness
* pre-…
Contacts