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Early Diagnosis and Early Treatment of Alzheimer's Disease Based on Senile Plaque Imaging

Early Diagnosis and Early Treatment of Alzheimer's Disease Based on Senile Plaque Imaging

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02931136
Enrollment
300
Registered
2016-10-12
Start date
2019-11-30
Completion date
2025-12-31
Last updated
2019-04-16

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

Conditions

Mild Cognitive Impairment, Biomarker, Diagnosis, Treatment

Brief summary

The purpose of this study is based on the Flutemetamol-PET senile plaque imaging to investigate the peripheral blood biochemical and brain MRI imaging biomarkers and to research completely independent intellectual property rights neuropsychological test tool for the MCI due to AD. At the same time, the investigators will study the efficacy and safety of early treatment of MCI due to AD by Huperzine A in 52 weeks.

Detailed description

This is a randmized, double-blind, placebo-controll study.

Interventions

The participants will treatment by the Huperzine A 200 ug/day in 52 weeks.

DRUGPlacebo

The participants will treatment by the placebo in 52 weeks.

Sponsors

Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* memory complaint, preferably corroborated by a spouse or relative. * objective memory impairment. * normal general cognitive function. * intact activities of daily living. * absence of dementia. * the positive of brain senile plaque.

Exclusion criteria

* more than two lacuna ischemia (of diameter \< 1 cm) as revealed by MRI fluid-attenuated inversion recovery (FLAIR) sequence. * other type of dementia except AD

Design outcomes

Primary

MeasureTime frame
The average annual conversion rate in patients of MCI due to AD convert to the AD.52 weeks

Countries

China

Contacts

Primary ContactTao Wang, M.D., Ph.D.
wtshhwy@163.com00862164387250

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026