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Clinical Study of GKT in Diabetes Related Dementia

Primary Purpose

Dementia

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ginkgo Ketone Ester Tablets
Sponsored by
Shanghai 10th People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dementia

Eligibility Criteria

65 Years - 85 Years (Older Adult)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Ginkgo Ketone Ester Tablets Treatment Group

    control group

    Arm Description

    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

    Outcomes

    Primary Outcome Measures

    Cognitive function testing
    Alzheimer's Disease Assessment Scale-Cognitive section (0-70), the higher the score, the more severe the cognitive impairment

    Secondary Outcome Measures

    Memory function assessment
    Auditory Word Learning Test (AVLT-H),the lower the score, the more severe the cognitive impairment
    Assessment of daily living ability
    Functional Activity Questionnaire (FAQ)S,the higher the score, the more severe the cognitive impairment
    Perform functional evaluation
    Shape Connection Test A and B (STT-A&B),the higher the score, the more severe the cognitive impairment
    Attention assessment
    Symbolic Digital Form Test (SDMT),the lower the score, the more severe the cognitive impairment

    Full Information

    First Posted
    April 10, 2023
    Last Updated
    July 27, 2023
    Sponsor
    Shanghai 10th People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05855863
    Brief Title
    Clinical Study of GKT in Diabetes Related Dementia
    Official Title
    Clinical Study of Ginkgo Biloba Ketone Ester Tablets in Diabetes Related Dementia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    June 30, 2026 (Anticipated)
    Study Completion Date
    June 30, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Shanghai 10th People's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No

    5. Study Description

    Brief Summary
    Recently a new clinical dementia subgroup based on brain imaging, called "diabetes related dementia (DrD)". DrD, unlike Alzheimer's disease and vascular dementia, is considered a "controllable" or "modifiable" form of dementia. However, there is currently a lack of corresponding treatment measures. Ginkgo biloba ketone ester tablets are extracts of Ginkgo biloba leaves. Previous studies have shown that they can increase cerebral blood flow, reduce cerebrovascular resistance, improve cerebral circulation, and are beneficial for the treatment of cognitive impairment. This project intends to explore the role of ginkgo ketoester tablets in diabetes related dementia through a multicenter randomized double-blind controlled clinical study.
    Detailed Description
    This study was divided into two treatment groups: the experimental group and the control group. 196 type 2 diabetes patients with mild cognitive impairmentpatients were randomly selected and assigned to the experimental group of 98 patients and the control group of 98 patients in a 1:1 equal amount. Experimental group: Ginkgo biloba ketone ester tablets combined with conventional hypoglycemic treatment group, the usage is Ginkgo biloba ketone ester tablets (Styron), taken orally, 3 times a day, 0.5g each time, and continuously administered for 6 months. Control group: conventional hypoglycemic treatment group. The Montreal Cognitive Assessment Basic (MoCA-B) was used for the detection of cognitive dysfunction. Neuropsychological testing of cognitive function was conducted using Alzheimer's Disease Assessment Scale - Cognitive Scale (ADAS-cog), Auditory Word Learning Test (AVLT-H);Assessment of Daily Living Ability - Functional Activity Questionnaire (FAQ);Shape Connection Test A and B and Symbolic Digital Form Test (SDMT).Collect patients' blood, and detect C-reactive protein, interleukin-6, oxidative stress, ApoE4 genotype, phosphorylated tau protein, irisin, β- Amyloid protein before and after the experiment.Detect changes in ankle brachial pulse wave conduction velocity (baPWV)/and ankle brachial blood pressure index (ABI) of patients before and after the experiment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Dementia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Masking Description
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    198 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Ginkgo Ketone Ester Tablets Treatment Group
    Arm Type
    Experimental
    Arm Description
    Ginkgo Ketone Ester Tablets (Styron), taken orally, 3 times a day, 0.5g each time, continuously administered for 6 months
    Arm Title
    control group
    Arm Type
    No Intervention
    Arm Description
    Conventional hypoglycemic therapy for 6 months
    Intervention Type
    Drug
    Intervention Name(s)
    Ginkgo Ketone Ester Tablets
    Other Intervention Name(s)
    styron
    Intervention Description
    Ginkgo Ketone Ester Tablets (Styron), taken orally, 3 times a day, 0.5g each time, continuously administered for 6 months
    Primary Outcome Measure Information:
    Title
    Cognitive function testing
    Description
    Alzheimer's Disease Assessment Scale-Cognitive section (0-70), the higher the score, the more severe the cognitive impairment
    Time Frame
    six months
    Secondary Outcome Measure Information:
    Title
    Memory function assessment
    Description
    Auditory Word Learning Test (AVLT-H),the lower the score, the more severe the cognitive impairment
    Time Frame
    six months
    Title
    Assessment of daily living ability
    Description
    Functional Activity Questionnaire (FAQ)S,the higher the score, the more severe the cognitive impairment
    Time Frame
    six months
    Title
    Perform functional evaluation
    Description
    Shape Connection Test A and B (STT-A&B),the higher the score, the more severe the cognitive impairment
    Time Frame
    six months
    Title
    Attention assessment
    Description
    Symbolic Digital Form Test (SDMT),the lower the score, the more severe the cognitive impairment
    Time Frame
    six months
    Other Pre-specified Outcome Measures:
    Title
    Concentration of C-reactive protein
    Description
    Human CRP(C-Reactive Protein) ELISA Kit for detecting C-reactive protein concentration (mg/L )in serum
    Time Frame
    six months
    Title
    Rate of arteriosclerosis in the large and middle arterial systems
    Description
    ankle brachial pulse wave conduction velocity (m/s )detected by Arteriosclerosis tester
    Time Frame
    six months
    Title
    Rate of arterial blockage in limbs
    Description
    ankle brachial blood pressure index (ABI) measures ankle blood pressure and upper arm brachial artery blood pressure through ankle brachial index instrument
    Time Frame
    six months
    Title
    Concentration of interleukin-6
    Description
    interleukin-6(IL-6) in serum detected by interleukin-6 ELISA Kit
    Time Frame
    six months
    Title
    Concentration of phosphorylation (p) - tau217
    Description
    Plasma phosphorylation (p) - tau217detected by P-Tau217 detection kit
    Time Frame
    six months
    Title
    Concentration of Amyloid protein Aβ 42/40
    Description
    Plasma Amyloid protein Aβ 42/40 detected by Aβ 42/40 detection kit
    Time Frame
    six months
    Title
    Participants with ApoE4 genotype
    Description
    ApoE4 genotype detected by ApoE4 genotype kit
    Time Frame
    six months
    Title
    Concentration of antioxidant enzyme activity
    Description
    Detection of glutathione peroxidase in serum
    Time Frame
    six months
    Title
    Concentration of oxidative stress
    Description
    Free radical detection in serum
    Time Frame
    six months
    Title
    Concentration of irisin
    Description
    Plasma irisin concentration detected by irisin ELISA kit
    Time Frame
    six months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    65 Years
    Maximum Age & Unit of Time
    85 Years
    Accepts Healthy Volunteers
    No
    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.

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    23594859
    Citation
    Fukazawa R, Hanyu H, Sato T, Shimizu S, Koyama S, Kanetaka H, Sakurai H, Iwamoto T. Subgroups of Alzheimer's disease associated with diabetes mellitus based on brain imaging. Dement Geriatr Cogn Disord. 2013;35(5-6):280-90. doi: 10.1159/000348407. Epub 2013 Apr 13.
    Results Reference
    result
    PubMed Identifier
    26289708
    Citation
    Hanyu H, Hirose D, Fukasawa R, Hatanaka H, Namioka N, Sakurai H. Guidelines for the Clinical Diagnosis of Diabetes Mellitus-Related Dementia. J Am Geriatr Soc. 2015 Aug;63(8):1721-3. doi: 10.1111/jgs.13581. No abstract available.
    Results Reference
    result
    PubMed Identifier
    25926349
    Citation
    Verdile G, Fuller SJ, Martins RN. The role of type 2 diabetes in neurodegeneration. Neurobiol Dis. 2015 Dec;84:22-38. doi: 10.1016/j.nbd.2015.04.008. Epub 2015 Apr 26.
    Results Reference
    result
    PubMed Identifier
    24405824
    Citation
    Fukasawa R, Hanyu H, Namioka N, Hatanaka H, Sato T, Sakurai H. Elevated inflammatory markers in diabetes-related dementia. Geriatr Gerontol Int. 2014 Jan;14(1):229-31. doi: 10.1111/ggi.12140. No abstract available.
    Results Reference
    result
    PubMed Identifier
    26531676
    Citation
    Hatanaka H, Hanyu H, Fukasawa R, Sato T, Shimizu S, Sakurai H. Peripheral oxidative stress markers in diabetes-related dementia. Geriatr Gerontol Int. 2016 Dec;16(12):1312-1318. doi: 10.1111/ggi.12645. Epub 2015 Nov 4.
    Results Reference
    result
    PubMed Identifier
    27109174
    Citation
    Hirose D, Hanyu H, Fukasawa R, Hatanaka H, Namioka N, Sakurai H. Frailty in diabetes-related dementia. Geriatr Gerontol Int. 2016 May;16(5):653-5. doi: 10.1111/ggi.12566. No abstract available.
    Results Reference
    result

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    Clinical Study of GKT in Diabetes Related Dementia

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