Skip to content

The Application of Stroop Test in the Diagnosis of Postoperative Neurocognitive Disorders in Elderly Patients

The effect of Esketamine on postoperative cognitive impairment in elderly patients: a randomized controlled clinical study based on the Stroop test

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071929
Enrollment
Unknown
Registered
2023-05-30
Start date
2023-05-30
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Postoperative Delirium

Interventions

Gold Standard:Neuropsychological tests were performed before and on the 3rd day after surgery, including the Speech Learning Test (VLT), the Wisconsin Card Sorting Test (SCWT), the Attachment Test (TM
Index test:Encephal App of stroop test

Sponsors

The Third Affiliated Hospital of Navy Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients who require surgical treatment in our hospital over 65 years old and with the ASA score of I-III, without color blindness, cognitive impairment, or chronic mental illness are included.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to participate in this study; 2. Patients with cognitive impairment on preoperative MMSE testing; 3. Patients who are unable to complete the standard diagnosis program of POCD; 4. Patients who are unable to communicate normally or have a history of serious central nervous system disease or mental illness, or have a history of brain surgery; 5. Patients who are taking neurological or psychiatric drugs; 6. Patients who are deemed unsuitable by researchers to participate in this project.

Design outcomes

Primary

MeasureTime frame
Sensitivity;specificity;accuracy;

Countries

China

Contacts

Public ContactKai Wei

The Third Affiliated Hospital of Navy Medical University

weikai_880325@163.com+86 159 2119 6809

Outcome results

None listed

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