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New treatment option for Cardiac Arrest
Official title Monitoring and Optimization of Cerebral Perfusion Pressure in Post-cardiac Arrest Patients: a Pilot Study
ClinicalTrials.gov ID: NCT06601842
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- non-traumatic cardiac arrest
- admitted to ICU
- GCS: motor \<=5
- severity: TIMECARD score medium-risk group
You likely can't join if
- traumatic cardiac arrest
- pregnancy
- intracranial hemorrhage
- coagulopathy
- anti-platelet or anti-coagulation use
- terminal illness
See the full eligibility criteria
- non-traumatic cardiac arrest
- admitted to ICU
- GCS: motor \<=5
- severity: TIMECARD score medium-risk group
- traumatic cardiac arrest
- pregnancy
- intracranial hemorrhage
- coagulopathy
- anti-platelet or anti-coagulation use
- terminal illness
- pre-arrest CPC score \>=3
- GWR \< 1.2 on CT or severe hypoxic ischemic encephalopathy
- CNS infection
The study team makes the final eligibility decision.
Where it's taking place
- Taipei, Taiwan
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Taipei, Taiwan. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.