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Postoperative Cognitive Dysfunction: Correlations With Olfactory Dysfunction and Related Gene Changes

H

Han Yuan

Status

Completed

Conditions

Postoperative Cognitive Dysfunction

Study type

Observational

Funder types

Other

Identifiers

NCT02992600
XYFY2016-KL018-01

Details and patient eligibility

About

To study on the Postoperative Cognitive Dysfunction: Correlations With Olfactory Dysfunction and Related Gene Changes.To explore whether the olfactory dysfunction could be used as a predictor of POCD and to provide reference for POCD prevention, early detection and timely diagnosis and treatment.

Enrollment

300 patients

Sex

All

Ages

60 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between 60 to 85 years old;
  • Undergoing non-cardiac and non-neurological surgery under general anesthesia;
  • Expected hospital stay ≥5 days;
  • American Society of Anesthesiologists class I or II.

Exclusion criteria

  • Mental or neurodegenerative diseases;
  • History of severe trauma or surgery within one year;
  • History of nasal or sinus illness or surgery;
  • Cold or influenza within 3 weeks;
  • Significant history of organ dysfunction;
  • Previous neuropsychological testing;
  • Difficulty to perform tests (including severe visual or auditory disorders);
  • Mini-Mental State Examination (MMSE) <24 points, <20 points if the participant only attended elementary school, or <17 points if the participant did not go to school.

Trial design

300 participants in 2 patient groups

study group
Description:
300 male and female patients undergoing non-cardiac surgery are enrolled at the Affiliated Hospital of Xuzhou Medical University \[Jiangsu China\]. Patients will be divided into POCD and non-POCD groups according to the scores of neuropsychological tests.
control group
Description:
30 healthy volunteers are enrolled for calculating the Z-scores of study group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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