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Evaluation and Mechanism Study on the Effect of Huanshaodan Combined with Feiteng Eight Methods in Treating Mild and Moderate Spleen and Kidney Deficiency Type Alzheimer's Disease Patients

Evaluation and Mechanism Study on the Effect of Huanshaodan Combined with Feiteng Eight Methods in Treating Mild and Moderate Spleen and Kidney Deficiency Type Alzheimer's Disease Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078951
Enrollment
Unknown
Registered
2023-12-21
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Alzheimer's disease

Interventions

Huanshaodan group:Oral rejuvenating pills
Control group:None
Acupuncture and moxibustion Therapy of Flying Eight Methods:Acupuncture and moxibustion Therapy of Flying Eight Methods
Acupuncture and moxibustion Therapy of Flying Eight Methods combined with HuanshaDan:Acupuncture and moxibustion Therapy of Flying Eight Methods combined with HuanshaDan

Sponsors

Chengdu Eighth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 95 Years

Inclusion criteria

Inclusion criteria: ? Age = 60 years old; ? Conforming to the diagnostic criteria for mild to moderate spleen kidney deficiency type of AD: Referring to the core clinical standards for AD dementia developed by the National Institute of Aging (NIA) and the Alzheimer's Association (AA) in the United States, the diagnosis is highly likely to be AD; Progressive memory or other cognitive impairment for = 3 months; MMSE score of the Simplified Mental State Scale: Illiteracy = 19 points; Primary school = 22 points, secondary school and above = 24 points; Clinical dementia rating (CDR) score = 1 point; Daily living ability ADL (14 items) score = 17 points; Using the Dementia Syndrome Classification Scale (SDSD) to screen AD patients with spleen and kidney deficiency; ? Willing to accept and cooperate with the implementation of this study; ? The expected check-in time is no less than three months.

Exclusion criteria

Exclusion criteria: ? Cognitive impairment caused by intracranial lesions, or other neurological diseases (such as Parkinson's, stroke, epilepsy, etc.); ? Currently undergoing other cognitive therapy; ? Suffering from chronic diseases that hinder exercise; ? Individuals with severe cardiovascular, cerebrovascular, digestive, blood, liver and kidney dysfunction, as well as serious complications; ? Individuals with visual and auditory impairments and communication difficulties; ? Other research participants who are participating in the study that affect the results of this study; ? Patients with severe sleep disorders, anxiety, depression, and other neurological disorders.

Design outcomes

Primary

MeasureTime frame
Mini-mental State Examination;Montreal Cognitive Assessment;Hospital Anxiety and Depression Scale;PSQI;

Secondary

MeasureTime frame
NFL;GFAP;P-tau217;TNF-a;IL-6;BDNF;Aß1-40;Aß1-42;

Countries

China

Contacts

Public ContactMaoquan Li; Yuzhe Fei

Chengdu Medical College; Chengdu Eighth People's Hospital

917604412@qq.com+86 189 8210 1823

Outcome results

None listed

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