Clinical Study of GKT in Diabetes Related Dementia
Dementia
About this trial
This is an interventional treatment trial for Dementia
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes with mild cognitive impairment patients aged 65 years or above; Able to cooperate in completing cognitive function testing; Patients who can swallow pills No previous history of acute stroke Exclusion Criteria: Type 1 diabetes; Acute cerebral infarction and myocardial infarction within 3 months; Severe liver and kidney dysfunction; Late stage malignant tumors; Thyroid dysfunction; Brain injury and cerebral hemorrhage within 3 months; Folic acid and/or vitamin B12 deficiency Patients who are currently using thrombin inhibitors, defibrillators (with unclear efficacy in ischemic stroke and increased risk of bleeding), antiplatelet drugs, blood activating and stasis resolving agents, and other ginkgo biloba leaf preparations (as they may affect the evaluation of the therapeutic effect of ginkgo biloba ester tablets in this trial), as well as other trial medications.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Ginkgo Ketone Ester Tablets Treatment Group
control group
Ginkgo Ketone Ester Tablets (Styron), taken orally, 3 times a day, 0.5g each time, continuously administered for 6 months
Conventional hypoglycemic therapy for 6 months