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Clinical Trials in China / NCT06660238
Starting soon Observational

PET-CT to Assess Brain Damage in Cardiac Arrest Patients

NCT06660238 · tracked via the Priya Life Science China tracker
Sponsor
Capital Medical University
Phase
Observational
Started
2025-05-01
Last updated
2025-04-11

Condition(s) studied

Cardiac ArrestBrain Injuries

Investigational drug(s) / intervention(s)

No interventions

No interventions: No interventions

Study summary

This was a single-center, observational study. Patients with successful cardiopulmonary resuscitation (CPR) will be transferred to the emergency intensive care unit for further standardized management. After successful return of spontaneous circulation (ROSC) for 72 hours and hemodynamic stability for 24 hours, the patients underwent positron emission computed tomography (PET-CT) examination after resuscitation. The supervising physician accompanied the patient and used monitors to monitor vital signs during the examination. Patients who were on ventilators were mechanically ventilated with a magnetic ventilator (HAMILTON-MRI, United States). In addition to conventional cerebral oxygen metabolism, cerebral blood flow, oxygen extraction fraction, cerebral blood volume and other indicators were added in this experiment. These indicators can evaluate the patient's cerebral metabolism, cerebral blood flow and cerebral blood oxygen damage degree. The neurological outcome was followed up 6 months after onset according to the cerebral performance category(CPC).

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * age ≥18 years. * sustained hemodynamic stability for ≥24h. * the patients were unconscious and not able to obey verbal commands. • Advanced life support and target temperature management within 6 hours of return of spontaneous circulation (ROSC). Exclusion Criteria: * Patients with hemodynamic instability. * Patients who could not complete cranial PET-CT examination for special reasons. • Patients during pregnancy. * Patients who combined traumatic brain injury, stroke, cerebral hemorrhage and other diseases. * Patients whose family members did not agree to be enrolled.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing chaoyang hospital Beijing Beijing Municipality

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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 NCT06660238 on ClinicalTrials.gov ↗ ← All trials in China