Efficacy of Chinese Traditional Medicine "Smart Soup" in Cognition and Behavior Regulation in Alzheimer's Disease

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05538507
Collaborator
Tongji University (Other)
180
1
6
24
7.5

Study Details

Study Description

Brief Summary

It is a prospective interventional randomized controlled single center trial. The goal of the trial is to evaluate the efficacy of smart soup on cognition, behavior, biomarkers and safety in Alzheimer's disease (aMCI and dementia).

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Alzheimer's disease (AD) is the most common cause of dementia and places a heavy burden on patients, families, society and healthcare. The drugs that have been marketed worldwide for the treatment of AD so far can only delay but not reverse the course of the disease, and the current drug development is all directed at a single target, while the onset of AD is the result of a combination of multiple factors, which is an important reason why so many drugs have faltered. The investigators need to find new multi-target intervention pathways from another perspective.

The advantage of Chinese medicine is multi-target and multi-factor regulation, which has advantages in treating complex diseases. The combination of ancient smart soup with donepezil was able to significantly improve the cognitive function in demented animals. Smart Soup is prepared from three herbs: Rhizoma Acori Tatarinowii, Poria cum Radix Pini, Radix Polygalae. These three herbs are each 15 grams and ground into a very fine powder. This approach reduced the formation of characteristic pathological changes at the pathological level, therefore, the combination of ancient Chinese medicine formulae with modern medical treatment may bring new hope to the treatment of demented patients.

The main design of this study are following: Patients over 40 years of age and eligible for NIA-AA 2011 probable AD and probable MCI were included in this study and were divided into 6 groups of 30 patients each. Group I AD patients were given donepezil 10 mg, memantine 20 mg and smart soup, group II AD patients were given donepezil 10 mg, memantine 20 mg and placebo; group III AD patients were given donepezil 10 mg and smart soup, group IV AD patients were given donepezil 10 mg and placebo; group V mild cognitive impairment (MCI) patients were given smart soup, and group VI MCI patients were given placebo.

Evaluations were set before enrollment, every three months till one year and the evaluators were single-blind. The scales involved in the evaluation of cognitive function and quality of life, sleep condition, and emotional behavior included ADAS-cog, MMSE, CDR, ADL, CMAI, NPI, and EQ-5D, which were evaluated five times. MRI, EEG, blood oxidative stress indicators, and biological markers were collected at the same time at enrollment and at the end of the study. Genotype collection was completed at enrollment. Safety was also evaluated with monthly testing of ECG, routine blood, liver and kidney function, urinary routine, and recording of side effects.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Patients were divided into 6 groups according to the enrollment criteria, with 30 cases in each group. Group I AD patients were given donepezil 10 mg, memantine 20 mg and smart soup, group II AD patients were given donepezil 10 mg, memantine 20 mg and placebo; group III AD patients were given donepezil 10 mg and smart soup, group IV AD patients were given donepezil 10 mg and and placebo; group V MCI patients were given smart soup, and group VI MCI patients were given placebo.Patients were divided into 6 groups according to the enrollment criteria, with 30 cases in each group. Group I AD patients were given donepezil 10 mg, memantine 20 mg and smart soup, group II AD patients were given donepezil 10 mg, memantine 20 mg and placebo; group III AD patients were given donepezil 10 mg and smart soup, group IV AD patients were given donepezil 10 mg and and placebo; group V MCI patients were given smart soup, and group VI MCI patients were given placebo.
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy of Chinese Traditional Medicine "Smart Soup" in Cognition and Behavior Regulation in Alzheimer's Disease
Actual Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group I severe AD

Patients over 40 years of age and eligible for NIA-AA 2011 probable severe AD will be given donepezil 10 mg, memantine 20 mg and smart soup

Drug: smart soup
Severe AD, mild or moderate AD and MCI will be given smart soup
Other Names:
  • traditional chinese medicine
  • Drug: Donepezil
    Severe AD and mild or moderate AD will be given donepezil
    Other Names:
  • donepezil pill
  • Drug: Memantine
    Severe AD will be given memantine
    Other Names:
  • Memantine Pill
  • Sham Comparator: Group II severe AD

    Patients over 40 years of age and eligible for NIA-AA 2011 probable severe AD will be given donepezil 10 mg, memantine 20 mg and placebo

    Drug: Donepezil
    Severe AD and mild or moderate AD will be given donepezil
    Other Names:
  • donepezil pill
  • Drug: Memantine
    Severe AD will be given memantine
    Other Names:
  • Memantine Pill
  • Drug: Placebo
    patients with MCI will be given placebo

    Active Comparator: Group III Mild or moderate AD

    Patients over 40 years of age and eligible for NIA-AA 2011 probable mild or moderate AD will be given donepezil 10 mg and smart soup

    Drug: smart soup
    Severe AD, mild or moderate AD and MCI will be given smart soup
    Other Names:
  • traditional chinese medicine
  • Drug: Donepezil
    Severe AD and mild or moderate AD will be given donepezil
    Other Names:
  • donepezil pill
  • Sham Comparator: Group IV Mild or moderate AD

    Patients over 40 years of age and eligible for NIA-AA 2011 probable mild or moderate AD will be given donepezil 10 mg and placebo

    Drug: Donepezil
    Severe AD and mild or moderate AD will be given donepezil
    Other Names:
  • donepezil pill
  • Drug: Placebo
    patients with MCI will be given placebo

    Active Comparator: Group V MCI

    Patients over 40 years of age and eligible for NIA-AA 2011 probable MCI will be given smart soup

    Drug: smart soup
    Severe AD, mild or moderate AD and MCI will be given smart soup
    Other Names:
  • traditional chinese medicine
  • Sham Comparator: Group VI MCI

    Patients over 40 years of age and eligible for NIA-AA 2011 probable MCI will be given placebo

    Drug: Placebo
    patients with MCI will be given placebo

    Outcome Measures

    Primary Outcome Measures

    1. Changes of cognitive screening [Through study completion, an average of 1 years]

      Using the neuropsychological scale, mini-mental state examination (MMSE,0-30), to assess every three months after trial entry

    2. Changes of comprehensive cognitive assessment [Through study completion, an average of 1 years]

      Use the neuropsychological scales, Alzheimer's Disease Assessment Scale-Cognitive section (ADAS-cog 0-75), to assess every three months after trial entry

    3. Changes in the degree of dementia [Through study completion, an average of 1 years]

      Use the neuropsychological scales, CDR(0-3), to assess every three months after trial entry

    4. Changes in behavior [Through study completion, an average of 1 years]

      Use the Cohen-Mansfield Agitation Inventory (CMAI,29-203) to assess every three months after trial entry

    5. Changes in Psychiatric symptoms [Through study completion, an average of 1 years]

      Use the Neuropsychiatric Index (NPI) to assess every three months after trial entry

    6. Changes of daily living skills [Through study completion, an average of 1 years]

      Use Activity of Daily Living Scale(ADL,20-80)to assess every three months after trial entry

    7. Changes in health status [Through study completion, an average of 1 years]

      Use EuroQoL 5-dimension (EQ-5D,0-100) to assess every three months after trial entry

    8. Tau and Beta-amyloid biomarkers in CSF and plasma [Through study completion, an average of 1 years]

      Concentration ( pg/mL) of beta-amyloid, tau and phospho-tau in cerebrospinal fluid (CSF) and plasma of patients with dementia and controls

    9. Magnetic resonance imaging and Electroencephalogram(EEG) [Through study completion, an average of 1 years]

      Evaluate the imaging and EEG changes of dementia patients. Specifically, EEG can be used to monitor the activity of brain waves in different parts of the cerebral cortex (e.g. power in alpha band, distribution and power of slow theta/delta waves etc.)

    10. Oxidative stress markers in blood [Through study completion, an average of 1 years]

      Concentration of Dopamine in blood of patients with dementia and controls

    11. Alterations of neurotransmitters in the blood [Through study completion, an average of 1 years]

      Concentration (ng/ml) of 5-hydroxy tryptamine (HT) in blood of patients with dementia and controls

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • NIA-AA 2011 AD probable Alzheimer's disease, mild to moderate, stable use donepezil 10mg/d for 3 months

    • NIA-AA 2011 AD probable Alzheimer's disease, severe, stable use donepezil 10mg/d and memantine 20mg/d for 3 months

    • NIA-AA 2011 MCI probable criteria

    • stable care giver

    • Traditional Chinese medicine diagnosis: pixu tanzhuo

    Exclusion Criteria:
    • Severe systemic disease (heart, liver ,kidney function failure)

    • contradictions of MRI examination

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Peking Union Medical College Hospital Beijing China

    Sponsors and Collaborators

    • Peking Union Medical College Hospital
    • Tongji University

    Investigators

    • Principal Investigator: Jing Gao, MD, Peking Union Medical College Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    gaojing, Professor, Department of Neurology, Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT05538507
    Other Study ID Numbers:
    • Smart Soup
    First Posted:
    Sep 14, 2022
    Last Update Posted:
    Sep 14, 2022
    Last Verified:
    Sep 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by gaojing, Professor, Department of Neurology, Peking Union Medical College Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 14, 2022