Clinical Trials Directory

Trials / Completed

CompletedNCT06694597

Efficacy, Safety of Astragalus Membranaceus in Mild-to-Moderate Alzheimer's Disease

Efficacy and Safety of Astragalus Membranaceus on the Improvement of Cognitive and Non-cognitive Symptoms in Mild-to-Moderate Alzheimer's Disease

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
76 (actual)
Sponsor
Fujian Medical University Union Hospital · Academic / Other
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Alzheimer's disease (AD), the most common cause of dementia, is characterized by cognitive impairment, mental and behavioural abnormalities, and social dysfunction. Current treatments can only delay the progression of AD, not cure it completely. In vitro studies have shown that Astragalus has toxic effects such as anti-hypoxia injury of nerve cells, anti-free radical damage, anti-excitatory amino acids, etc. It can be used to expand cerebral vessels, increase cerebral blood flow, improve cerebral microcirculation, protect brain cells, and repair damaged brain cells. However, the clinical effects of add-on Astragalus in improving cognition in these patients remain unclear. Therefore, this pragmatic clinical trial aims to determine the efficacy and safety of add-on Astragalus in improving cognition in patients with AD

Conditions

Interventions

TypeNameDescription
DRUGAstragalus Membranaceus RootAstragalus tablets 15g, warm water to drink, once a day, take for 1 year, during which routine treatment should also be carried out.

Timeline

Start date
2023-05-01
Primary completion
2024-03-31
Completion
2024-03-31
First posted
2024-11-19
Last updated
2024-11-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06694597. Inclusion in this directory is not an endorsement.