Biomarkers and Risk Factors for Perioperative Neurocognitive Dysfunction in Elderly Patients
- Conditions
- Perioperative Neurocognitive Dysfunction
- Interventions
- Diagnostic Test: Pittsburgh sleep quality indexDiagnostic Test: Self-rating depression scaleDiagnostic Test: Montreal Cognitive Assessment
- Registration Number
- NCT06044207
- Lead Sponsor
- Jinan Central Hospital
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 1000
- Age more than or equal to 65 years old
- ASA classification Ⅰ~Ⅲ grade
- History of previous Craniocerebral surgery or Craniocerebral trauma
- Inability to successfully complete preoperative psychological function tests
- Those who are severely deaf, speech impaired and otherwise unable to communicate.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Patients without perioperative neurocognitive dysfunction Pittsburgh sleep quality index - Patients with perioperative neurocognitive dysfunction Pittsburgh sleep quality index - Patients without perioperative neurocognitive dysfunction Self-rating depression scale - Patients with perioperative neurocognitive dysfunction Montreal Cognitive Assessment - Patients without perioperative neurocognitive dysfunction Montreal Cognitive Assessment - Patients with perioperative neurocognitive dysfunction Self-rating depression scale -
- Primary Outcome Measures
Name Time Method Perioperative neurocognitive dysfunction 1 year postoperative Identification of patients who develop perioperative neurocognitive disorders after surgery by postoperative follow-up with cognitive function tests
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Jinan Central Hospital
🇨🇳Jinan, Shandong, China