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Research for the effects of statins on cognitive function

Research for the effects of statins on cognitive function

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029036
Enrollment
Unknown
Registered
2020-01-12
Start date
2020-02-03
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular disease and cognitive function

Interventions

Case series:no

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1. All selected patients meet the primary prevention and secondary prevention standards for cardiovascular disease by taking statins; 2. Have sufficient visual and auditory discrimination ability to undergo cognitive assessment; 3. The mental state and intelligence are normal, which can cooperate with the development of the cognitive scale assessment work; 4. Informed consent and voluntary interview.

Exclusion criteria

Exclusion criteria: 1. Hearing, disturbance of consciousness, severe mental illness or history of mental illness; 2. Patients with diagnosed or suspected cognitive impairment (in addition to organic diseases, also include neurasthenia, hysteria, depression, schizophrenia, mania, reactive psychosis, etc.), dementia High-risk population (stroke patients) and dementia patients: Alzheimer's disease patients diagnosed; patients with other dementia diseases such as Parkinson's disease, Huntington's disease, vascular dementia or frontotemporal dementia; brain tumors, bacteria Meningitis and other brain infections, encephalitis, brain degeneration, traumatic brain injury, epilepsy, schizophrenia, history of electrical shock treatment, cognitive impairment related to mental retardation, autism, Down syndrome or delirium; 3. People who are allergic to statins or any component of statins; 4. Patients with active liver disease, including patients with unexplained persistent elevation of serum transaminase and any serum transaminase elevation exceeding 3 times the upper limit of normal value (ULN); patients with decompensated cirrhosis and acute liver failure; biliary occlusion Patient; Patients with severe renal impairment (creatinine clearance <30 ml / min); 6. Patients with myopathy (including myositis); 7. Patients who are concurrently using cyclosporin; 8. During pregnancy, breastfeeding, and women who may become pregnant without proper contraception; 9. Patients with malignant tumors and end-stage disease (end-stage survival time <1 year); 10. Patients who cannot participate in follow-up; 11. Those who are unwilling to accept this investigation or cannot cooperate for other reasons.

Design outcomes

Primary

MeasureTime frame
MMSE or MoCa Cognitive Assessment Scale;

Countries

China

Contacts

Public ContactZhang Jin

The First Hospital of Lanzhou University

chzhangjin@163.com+86 18919808653

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026