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Clinical Trials in China / NCT07643194
Starting soon Observational

Cohort Study of Postoperative Cognitive Dysfunction After Off-Pump Coronary Artery Bypass Grafting

NCT07643194 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Anzhen Hospital
Phase
Observational
Started
2026-05-24
Last updated
2026-06-11

Condition(s) studied

Postoperative Cognitive Dysfunction (POCD)

Investigational drug(s) / intervention(s)

Off-Pump Coronary Artery Bypass Grafting

Off-Pump Coronary Artery Bypass Grafting: Off-pump coronary artery bypass grafting is performed as part of routine clinical care for patients with coronary artery disease. The study protocol does not assign participants to this procedure or to any additional intervention. This observational study will collect perioperative clinical data and follow patients after surgery to assess postoperative cognitive dysfunction.

Study summary

This prospective cohort study aims to investigate postoperative cognitive dysfunction in patients undergoing off-pump coronary artery bypass grafting. Eligible patients will be enrolled before surgery and followed after surgery. Cognitive function will be assessed using the Montreal Cognitive Assessment before surgery and at predefined postoperative time points. Perioperative clinical information, including preoperative assessment data, intraoperative monitoring parameters, and postoperative clinical data, will be collected. The study will evaluate the occurrence of postoperative cognitive dysfunction and explore its association with perioperative factors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older * Scheduled to undergo elective off-pump coronary artery bypass grafting * American Society of Anesthesiologists physical status classification I to IV * Able to complete preoperative cognitive assessments, including the Mini-Mental State Examination and the Montreal Cognitive Assessment * Written informed consent provided by the patient or family member Exclusion Criteria: * Emergency surgery * Pre-existing diagnosed cognitive impairment or history of psychiatric disease * Preoperative cognitive impairment * Severe neurological disease, such as sequelae of stroke, that may interfere with cognitive assessment * Severe visual or hearing impairment that prevents completion of cognitive assessment * Inability to understand Chinese or presence of language communication barriers

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing Anzhen Hospital, Capital Medical University Beijing Beijing Municipality

More Beijing Anzhen Hospital trials in China

Other trials for the same condition

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 NCT07643194 on ClinicalTrials.gov ↗ ← All trials in China