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RECRUITING
NCT06601842
NA

Monitoring and Optimization of Cerebral Perfusion Pressure in Post-cardiac Arrest Patients: a Pilot Study

Sponsor: National Taiwan University Hospital

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2024-12-10

Completion Date

2026-12

Last Updated

2024-12-16

Healthy Volunteers

No

Conditions

Interventions

DEVICE

ICP monitoring

ICP monitoring

Locations (1)

National Taiwan University Hospital

Taipei, Taiwan