Postoperative Cognitive Dysfunction Clinical Trial
Official title:
Correlation Between Postoperative Cognitive Dysfunction and Telomere Length in Patients With Non-cardiac Surgery
| 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 |
To study on the Postoperative Cognitive Dysfunction: Correlations With Leukocyte telomere length。
| 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. |
| Country | Name | City | State |
|---|---|---|---|
| China | Department of Anesthesia of the Affiliated Hospital of Xuzhou Medical University | Xuzhou | Jiangsu |
| Lead Sponsor | Collaborator |
|---|---|
| Xuzhou Medical University |
China,
| 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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