Serial multiomics profiling using serum and cerebrospinal fluid samples following out-of-hospital cardiac arrest: a prospective observational study
NCT ID NCT07090577
First seen Sep 10, 2026 · Last updated Sep 10, 2026
Summary
The goal of this observational study is to identify further pathophysiologic mechanism of secondary brain injury following cardiac arrest by using serial multiomics profiling of serum and cerebrospinal fluid (CSF) samples. The main question it aims to answer is: A. The main question it aims to answer is: What are the dynamic molecular changes in serum and CSF that reflect the pathophysiological mechanisms of secondary brain injury after cardiac arrest? B. What are the differences in serum and CSF multiomic signatures between varying severities of cardiac arrest, and how are these differences associated with the underlying pathophysiological mechanisms of secondary brain injury? Serum and CSF samples that have already been prospectively collected from participants and stored in the BioBank will be used for this analysis.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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15 people
The number who actually took part.
- Started
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Jul 2025
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients with an out-of-hospital cardiac arrest who underwent post-resuscitation care
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years old * Out-of-hospital cardiac arrest (OHCA) * Patients who have received post-resuscitation care including temperature control due to unconsciousness (Glasgow Coma Score \< 8) after sustained ROSC. * Patients who consented to the placement of lumbar catheter for storing cerebrospinal fluid and blood samples in a human biobank. Exclusion Criteria: * Patients diagnosed with a central nervous system-related disease before cardiac arrest * Patients who have undergone extracorporeal circulatory membrane oxygenation therapy * Patients who died within 24 hours from post-resuscitation care
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Chungnam National University Hospital
Daejeon, 35015, South Korea
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Other studies related to the condition(s) this trial covers.
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