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NCT07369466Not yet recruiting

Association of Preoperative Hippocampal Glucose Metabolism With Postoperative Delirium in Older Diabetic Patients

Preoperative Hippocampal Glucose Metabolism Levels and the Risk of Postoperative Delirium in Older Patients With Type 2 Diabetes: A Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 27 Jan 2026

Brief summary (registry, in English)

Objective: To investigate the association between preoperative hippocampal glucose metabolism levels and the risk of postoperative delirium (POD) in elderly patients with type 2 diabetes (T2DM), and to provide a prospective neuroimaging biomarker for identifying high-risk populations. Methods: This prospective cohort study plans to enroll 154 elderly T2DM patients scheduled for liver tumor resection at the First Medical Center of Chinese PLA General Hospital. Baseline cognitive function will be assessed using the Mini-Mental State Examination (MMSE) one day before surgery. Hippocampal glucose metabolism will be quantitatively evaluated by measuring the mean standardized uptake value (SUVmean) of bilateral hippocampi using ¹⁸F-FDG PET/CT. POD will be assessed twice daily from postoperative days 1 to 7 using the 3-Minute Diagnostic Interview for CAM (3D-CAM). The correlation between preoperative hippocampal SUVmean and POD incidence will be analyzed using univariate and multivariate logistic regression models. The predictive performance will be evaluated by constructing receiver operating characteristic (ROC) curves. Furthermore, the relationship between a peripheral insulin resistance marker (the triglyceride-glucose index, TyG index) and hippocampal metabolism levels will be analyzed. Significance: This study aims to determine whether impaired preoperative hippocampal metabolism serves as an independent risk factor for POD. The findings are expected to provide a prospective functional neuroimaging biomarker for the early warning of POD and offer a theoretical basis for developing precise prevention strategies targeting cerebral metabolic abnormalities. This will facilitate the application of neuroimaging techniques in the field of perioperative brain dysfunction monitoring.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
154 (estimated)
First submitted
10 Jan 2026
Start date
1 Feb 2026
Primary completion date
1 Feb 2028
Lead sponsor
Chinese PLA General Hospital
NCT number
NCT07369466

What you commit to

  • Study type: Observational
  • Planned participants: 154
  • From 1 Feb 2026 to the primary completion date, 1 Feb 2028
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of organic brain disorders, including stroke, traumatic brain injury, or intracranial tumors.
  • History of psychiatric disorders or current use of antipsychotic medications.

Other

  • Patient declines to participate.
  • Inability to cooperate with cognitive assessments or a preoperative Mini-Mental State Examination (MMSE) score \< 23.
  • American Society of Anesthesiologists (ASA) physical status classification ≥ IV.

Who the study is looking for

  • Diagnosed with type 2 diabetes mellitus (T2DM).
  • Age ≥ 65 years.
  • Scheduled for elective liver tumor resection surgery with an expected operative duration \> 2 hours.
  • Underwent whole-body ¹⁸F-FDG PET/CT scan within 1 month prior to surgery.

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.