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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03703973
Other study ID # POCDLTL
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2016
Est. completion date December 31, 2020

Study information

Verified date October 2018
Source Xuzhou Medical University
Contact Junli Cao
Phone +86 15162160809
Email caojl0310@yahoo.com.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To study on the Postoperative Cognitive Dysfunction: Correlations With Leukocyte telomere length。


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 85 Years
Eligibility Inclusion Criteria:

- Non-cardiac surgery patients;

- Age is greater than or equal to 65 years old;

- Han Nationality, mother tongue is chinese;

?The MMSE score:Illiteracy is greater than or equal to 17 points, primary school is greater than or equal to 20 points, higher secondary school is more than 24 points;

?The Geriatric Depression Scale (GDS) grade 1 or 2;

?The important function without serious heart, brain, liver, kidney, lung and other organs;

- The ASA class I or II;

- The people signed informed consent.

Exclusion Criteria:

- The diagnosis of neurological and psychiatric disorders, such as Alzheimer's disease, Parkinson's syndrome, multiple sclerosis, schizophrenia, depression, etc.; ?Had severe head and face disease, trauma history or history of surgery;

- Had a history of influenza in 3 weeks; ?The serious body disease and tobacco, wine and other substance abuse history; ?The presence of malignant tumor with shorter survival disease.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Neuropsychology test
We do the neuropsychological tests, Mini-Mental score examination (MMSE) and olfaction test 1 day before (baseline) and 1 week,3 months,1 year and 3 years after surgery without safety issue.

Locations

Country Name City State
China Department of Anesthesia of the Affiliated Hospital of Xuzhou Medical University Xuzhou Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Xuzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the neuropsychological test to measure cognitive function 1 day before surgery(baseline)
Primary Mini-Mental score examination [MMSE] used for screening of dementia 1 day before surgery(baseline)
Primary the leukocyte telomere length on the surgery day
Primary the neuropsychological test to measure cognitive function within the first 7 days (plus or minus 2 days) after surgery
Primary Mini-Mental score examination [MMSE] used for screening of dementia within the first 7 days (plus or minus 2 days) after surgery
Primary the neuropsychological test to measure cognitive function within the first 3 months (plus or minus 1 month) after surgery
Primary Mini-Mental score examination [MMSE] used for screening of dementia within the first 3 months (plus or minus 1 month) after surgery
Primary the neuropsychological test to measure cognitive function within the first 1 year (plus or minus 3 months) after surgery
Primary Mini-Mental score examination [MMSE] used for screening of dementia within the first 1 year (plus or minus 3 months) after surgery
Primary the neuropsychological test to measure cognitive function within the first 3 years (plus or minus 1 year) after surgery
Primary Mini-Mental score examination [MMSE] used for screening of dementia within the first 3 years (plus or minus 1 year) after surgery
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