Alzheimer Disease Clinical Trial
Official title:
Efficacy of Chinese Traditional Medicine "Smart Soup" in Cognition and Behavior Regulation in Alzheimer's Disease
NCT number | NCT05538507 |
Other study ID # | Smart Soup |
Secondary ID | |
Status | Recruiting |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | June 1, 2022 |
Est. completion date | June 2024 |
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).
Status | Recruiting |
Enrollment | 180 |
Est. completion date | June 2024 |
Est. primary completion date | June 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 90 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
China | Peking Union Medical College Hospital | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking Union Medical College Hospital | Tongji University |
China,
Hou Y, Wang Y, Zhao J, Li X, Cui J, Ding J, Wang Y, Zeng X, Ling Y, Shen X, Chen S, Huang C, Pei G. Smart Soup, a traditional Chinese medicine formula, ameliorates amyloid pathology and related cognitive deficits. PLoS One. 2014 Nov 11;9(11):e111215. doi: 10.1371/journal.pone.0111215. eCollection 2014. Erratum in: PLoS One. 2020 Aug 3;15(8):e0237035. — View Citation
Ling Y, Li Z, Chen M, Sun Z, Fan M, Huang C. Analysis of multiple constituents in Cong-Ming-Tang, a Chinese herbal formula for the treatment of amnesia, by high-performance liquid chromatography with quadrupole time-of-flight mass spectrometry. Phytochem Anal. 2013 Nov-Dec;24(6):677-88. doi: 10.1002/pca.2454. Epub 2013 Jul 9. — View Citation
McKhann GM, Knopman DS, Chertkow H, Hyman BT, Jack CR Jr, Kawas CH, Klunk WE, Koroshetz WJ, Manly JJ, Mayeux R, Mohs RC, Morris JC, Rossor MN, Scheltens P, Carrillo MC, Thies B, Weintraub S, Phelps CH. The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers Dement. 2011 May;7(3):263-9. doi: 10.1016/j.jalz.2011.03.005. Epub 2011 Apr 21. — View Citation
Wang Y, Wang Y, Sui Y, Yu H, Shen X, Chen S, Pei G, Zhao J, Ding J. The combination of aricept with a traditional Chinese medicine formula, smart soup, may be a novel way to treat Alzheimer's disease. J Alzheimers Dis. 2015;45(4):1185-95. doi: 10.3233/JAD-143183. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes of cognitive screening | Using the neuropsychological scale, mini-mental state examination (MMSE,0-30), to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes of comprehensive cognitive assessment | Use the neuropsychological scales, Alzheimer's Disease Assessment Scale-Cognitive section (ADAS-cog 0-75), to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes in the degree of dementia | Use the neuropsychological scales, CDR(0-3), to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes in behavior | Use the Cohen-Mansfield Agitation Inventory (CMAI,29-203) to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes in Psychiatric symptoms | Use the Neuropsychiatric Index (NPI) to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes of daily living skills | Use Activity of Daily Living Scale(ADL,20-80)to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Changes in health status | Use EuroQoL 5-dimension (EQ-5D,0-100) to assess every three months after trial entry | Through study completion, an average of 1 years | |
Primary | Tau and Beta-amyloid biomarkers in CSF and plasma | Concentration ( pg/mL) of beta-amyloid, tau and phospho-tau in cerebrospinal fluid (CSF) and plasma of patients with dementia and controls | Through study completion, an average of 1 years | |
Primary | Magnetic resonance imaging and Electroencephalogram(EEG) | 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.) | Through study completion, an average of 1 years | |
Primary | Oxidative stress markers in blood | Concentration of Dopamine in blood of patients with dementia and controls | Through study completion, an average of 1 years | |
Primary | Alterations of neurotransmitters in the blood | Concentration (ng/ml) of 5-hydroxy tryptamine (HT) in blood of patients with dementia and controls | Through study completion, an average of 1 years |
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