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Clinical Trials in China / NCT07239648
Recruiting Observational

Postoperative Delirium in Patients Undergoing Cardiac Surgery

NCT07239648 · tracked via the Priya Life Science China tracker
Sponsor
Xijing Hospital
Phase
Observational
Started
2025-10-31
Last updated
2026-08-04

Condition(s) studied

Postoperative Delirium

Investigational drug(s) / intervention(s)

Serum metabolic profile

Serum metabolic profile: Venous serum samples are analyzed for serum metabolic profiles or other test

Study summary

Establish a follow-up database for postoperative delirium in cardiac surgery patients, adopt a bidirectional cohort design to simultaneously analyze the associations between "preoperative exposure factors and postoperative delirium incidence" and "postoperative delirium and long-term adverse outcomes", and clarify the predictive factors and prognostic impacts of postoperative delirium.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. 18 years old and above 2. Patients undergoing elective cardiac surgery Exclusion Criteria: 1. Organ transplantation surgery 2. Pregnant patients 3. Diagnosed with dementia or mental illness (such as schizophrenia) before surgery

Primary outcome measure(s)

  • postoperative delirium — within 1 week after operation
    accessed by CAM-ICU/3D-CAM

Trial sites (1)

FacilityCityRegionStatus
Xijing Hospital Xi'an Shaanxi Recruiting

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Other trials for the same condition

Mechanisms and Intervention Strategies of Perioperative Glycemic Variability on Postoperative Delirium Recruiting
The Effect of Bupivacaine Liposome Preemptive Analgesia on Postoperative Pain and Delirium in Elderly Patients Undergoing Hip Fracture Surgery Starting soon
Association Between Local Cerebral Oxygenation Monitoring and Postoperative Delirium in Carotid Endarterectomy Recruiting
Correlation Analysis of POD and pNCD in Elderly Patients With Gastrointestinal Neoplasms Recruiting
Dynamic Multimodal Delirium Warning After Cardiac Surgery Starting soon
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07239648 on ClinicalTrials.gov ↗ ← All trials in China