The Association Between Postoperative Inflammatory and Neurological Serum Biomarker Concentrations and Occurrence of Postoperative Delirium

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Conditions studied: Delirium - Postoperative, Neuronal Damage, Blood Brain Barrier Defect, Postoperative Complications, Inflammation

In brief

Postoperative delirium is a frequent and serious complication in older surgical patients, linked to prolonged hospitalization and long-term cognitive decline. The pathogenesis of delirium possibly includes inflammation and blood-brain barrier disruption. Early identification of at-risk patients is limited by the lack of reliable biomarkers. Therefore, we will evaluate as our primary aim the association between S100B measured within 2 hours after surgery and the occurrence of postoperative delirium within the first three postoperative days in patients over the age of 65 undergoing major non-cardiac, non-intracranial and non-vascular surgery. We will further evaluate the association between NSE, IL-6 and Copeptin concentrations, measured within 2 hours after surgery, on the occurrence of delirium within the first three postoperative days. We will also evaluate the predictive value of S100B, NSE, IL-6 and Copeptin concentrations, measured within 2 hours after surgery, on the occurrence of delirium within the first three postoperative days. We will measure S100B, NSE, IL-6, and Copeptin preoperatively, within two hours after surgery and daily for the first three postoperative days. Delirium will be assessed twice daily in the morning and evening for the first three postoperative days. In the course of this study we will establish a biobank of plasma and serum samples of patients, which are drawn preoperatively and within the first two hours after surgery.

Key facts

Study ID

NCT07411612

Run by

Medical University of Vienna

People needed

1170

Starts

2026-01-12

Expected to finish

2030-01-18

Last updated by the study team

2026-02-17

Who can join

Age: 65 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provide written informed consent
• ≥ 65 years of age
• Scheduled for elective major non-cardiac, non-intrcranial, non-vascular surgery with estimated time of surgery ≥ 2 hours

You may not qualify if…

• Patients undergoing emergency surgery
• History of diagnosed dementia
• Language, vision, or hearing impairments that may compromise cognitive assessments
• Preoperative delirium
• ICU patients undergoing surgery

Where it is running

• Medical University of Vienna — Vienna, Austria (enrolling)

Full record on ClinicalTrials.gov

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