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Prospective Cohort Study on Influencing Factors of Differential Cognitive Outcomes in Perioperative Patients Undergoing CEA Surgery

Prospective Cohort Study on Influencing Factors of Differential Cognitive Outcomes in Perioperative Patients Undergoing CEA Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104090
Enrollment
Unknown
Registered
2025-06-10
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Postoperative cognitive decline

Interventions

Observation group:None

Sponsors

Department of Anaesthesiology, Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for elective CEA under general anesthesia 2.Age >= 60 years 3.ASA physical status I–III 4.No dementia 5.No severe hearing/visual impairment, language disorder, or communication difficulties. 6.Not concurrently participating in other clinical trials 7.Willing to participate in this study

Exclusion criteria

Exclusion criteria: 1.Abnormal Activities of Daily Living (ADL) score 2.Alcohol or drug dependence 3.Cognitive impairment caused by other conditions (e.g., traumatic brain injury, neurodegenerative diseases, etc.) 4.Patients with severe comorbidities (e.g., major cardiovascular, hepatic, renal, or hematologic diseases) or a history of delirium/psychiatric disorders

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Secondary

MeasureTime frame
Postoperative Delirium;Postoperative pain intensity;

Countries

China

Contacts

Public ContactZhengqian Li

Peking University Third Hospital

zhengqianli@hsc.pku.edu.cn+86 156 1190 8458

Outcome results

None listed

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