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Clinical Trial Summary

Basic information and biological samples of patients were collected preoperatively and intraoperatively, and patients were divided into case and control groups by cognitive function assessment postoperatively, and risk factors and biomarkers of perioperative cognitive dysfunction were derived by analyzing and statistically processing basic information and biological samples.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06044207
Study type Observational
Source Jinan Central Hospital
Contact Wenying Chi, Master
Phone 18654557772
Email cwy2907@zxyy.cn
Status Recruiting
Phase
Start date June 1, 2023
Completion date January 1, 2026