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A prospective cohort study of long-term cognitive dysfunction associated with sepsis

A prospective cohort study of long-term cognitive dysfunction associated with sepsis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086446
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cognitive dysfunction associated with sepsis

Interventions

Control group:NA

Sponsors

The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi Medical center of Nanjing Medical University.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Inclusion criteria for the sepsis group: The diagnostic criteria for sepsis set out in the Save Sepsis Campaign (SSC) guidelines published by the European Society of Critical Care Medicine and the American Society of Critical Care Medicine (ESICM/SCCM) in 2021 were met. 2) Inclusion criteria of control group: non-sepsis patients admitted during the same period.

Exclusion criteria

Exclusion criteria: 1. Have a history of neuropsychiatric diseases, such as cerebrovascular disease, central nervous system infection, dementia, epilepsy, Parkinson's disease, craniocerebral trauma surgery, etc., or the admission to the ICU with the above neuropsychiatric diseases; 2. Patients after cardiopulmonary resuscitation; 3. A history of coma or cognitive dysfunction before onset; 4. People with low intelligence and below primary school education; 5. Patients with history of hepatic encephalopathy, pulmonary encephalopathy, renal encephalopathy, hypothyroidism, etc.; 6. severe deafness, visual impairment, inability to communicate properly, etc., can not cooperate with the completion of the study related scale assessment; 7. A history of drug abuse, drug use, alcoholism and long-term use of psychotropic drugs; 8. Pregnant and/or lactating women; 9. Age =18 years or =80 years.

Design outcomes

Primary

MeasureTime frame
Cognitive function scale;Head MRI image;

Secondary

MeasureTime frame
NLRP3;Gut microbiota;

Countries

China

Contacts

Public ContactHui Jiaojie

The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi Medical center of Nanjing Medical University.

huijiaojie15@163.com+86 510 8535 0031

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026