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Clinical Trials in South Korea / NCT05830422
Enrolling by invitation Observational

Prediction of Delayed Cognitive Impairment in Cardiac Arrest Survivors With Good Neurological Outcomes

NCT05830422 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2023-11-01
Last updated
2024-02-09

Condition(s) studied

Cardiac Arrest, Out-Of-HospitalCognitive Impairment

Investigational drug(s) / intervention(s)

nothing

nothing: Follow-up observation was conducted without any intervention in an outpatient setting.

Study summary

The objective of this observational study is to provide basic data for predicting and analyzing the occurrence and causes of delayed cognitive impairment, an important factor in the quality of life, among discharged patients who have received targeted temperature management therapy and experienced favorable neurological outcomes after out-of-hospital cardiac arrest.

The main questions it aims to answer are:

* Can we identify abnormal areas in the brains of patients with delayed cognitive impairment using Brain MRI or positron emission tomography (PET) imaging?
* Is it possible to predict delayed cognitive impairment using biomarkers?

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients who visited the hospital emergency room due to cardiac arrest within 60 months after Institutional Review Board (IRB) approval * Patients with Glasgow Coma Scale (GCS) less than 8 points after spontaneous circulation recovery * Patients who are 18 years old or older * Patients who underwent targeted temperature management (TTM) * Patients who showed good neurological outcomes with CPC 1-2 points after evaluating the prognosis on days 10-14 after ROSC Exclusion Criteria: * Under 18 years of age * cardiac arrest cause is trauma * Patients who have not undergone targeted temperature management * Patients treated with extracorporeal membrane oxygenation (ECMO) * Patients who were not able to undergo SNSB testing * Patients who could not be followed up until 6 months after ROSC

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
박정수 Daejeon Seo-gu

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05830422 on ClinicalTrials.gov ↗ ← All trials in South Korea