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Clinical Trials in China / NCT07760415
Starting soon Observational

EEG Changes and Cognitive Profiles in Sepsis Patients With Different Inflammatory Phenotypes

NCT07760415 · tracked via the Priya Life Science China tracker
Sponsor
Xiangya Hospital of Central South University
Phase
Observational
Started
2026-08-01
Last updated
2026-08-12

Condition(s) studied

SepsisSepsis Associated EncephalopathySepsis and Septic ShockSepsis at Intensive Care Unit

Investigational drug(s) / intervention(s)

EEG monitoring

EEG monitoring: Standard sepsis bundle treatment + 72-hour quantitative continuous EEG monitoring + structured long-term cognitive follow-up.

Study summary

To characterize the electroencephalogram (EEG) features of sepsis patients with distinct inflammatory response phenotypes, dynamically track their evolutionary trajectories, and analyze their associations with long-term changes in cognitive function.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years and ≤90 years * First-time admission to the Intensive Care Unit (ICU) * Diagnosis of sepsis according to Sepsis-3.0 criteria (documented or clinically suspected infection plus Sequential Organ Failure Assessment \[SOFA\] score ≥2 points) * Expected ICU survival time ≥24 hours * Written informed consent provided by the patient or legal surrogate Exclusion Criteria: * Pregnancy or lactation * Cardiopulmonary-cerebral resuscitation (CPCR) performed during the current hospital admission * Pre-existing primary central nervous system (CNS) diseases, including: Acute cerebrovascular disease (e.g., hemiplegia, cranial nerve palsy) Central nervous system infection (e.g., pleocytosis in cerebrospinal fluid) Organic or metabolic encephalopathy (e.g., hepatic, renal, pulmonary, pancreatic, or severe inherited metabolic disorders) Drug-related encephalopathy (e.g., antipsychotic-associated encephalopathy, serotonin syndrome, neurotoxic antibiotics) Other structural or immunological brain diseases (e.g., traumatic brain injury, intracranial neoplasm, autoimmune encephalopathy) \- Inability to cooperate with or tolerate scalp EEG electrode placement (e.g., extensive scalp trauma or open scalp infection)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Xiangya Hospital of Central South University Changsha Hunan

More Xiangya Hospital of Central South University trials in China

Other trials for the same condition

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 NCT07760415 on ClinicalTrials.gov ↗ ← All trials in China