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Research on the Intervention Effect of Western Medicine on Preclinical AD: a Randomized Controlled Trial.

Research on the Intervention Effect of Western Medicine on Preclinical AD: a Randomized Controlled Trial.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052254
Enrollment
Unknown
Registered
2021-10-23
Start date
2018-09-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Alzheimer's disease

Interventions

971Group:Take 971 Targeting Aß Manno-oligosaccharide Diacid Capsules orally
Rivastigmine group:Take rivastigmine orally
Placebo group:Take placebo group orally

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Outpatients or inpatients aged 50-80 years and elderly residents of the community, regardless of gender, education level >= 6 years; 2. According to the neuropsychological scale and clinical symptoms, it is determined that there is cognitive impairment; 3. The subjects have not used other drugs that improve cognitive impairment before the test; 4. Diagnostic criteria: MCI (CDR=0.5) or mild Alzheimer's disease (CDR=1 point).

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, liver, and renal insufficiency (Note: severe liver insufficiency refers to ALT value > 2 times the upper limit of normal or AST value > 2 times the upper limit of normal; severe renal insufficiency refers to creatinine value > 1.5 times the upper limit of normal); 2. Participants with other mental and nervous system diseases and malignant tumors; 3. Geriatric Depression Scale (GDS) score < 10 points, excluding cognitive impairment caused by depression; 4. Those who have poor compliance or are dying of life and cannot complete the course of treatment; 5. Use other cognitive improvement drugs such as ChEIs or other psychotropic drugs within the past three months; 6. Those who are participating in other clinical drug trials.

Design outcomes

Primary

MeasureTime frame
AVLT score;

Secondary

MeasureTime frame
ADAS-cog/MMSE score;

Countries

China

Contacts

Public ContactSun Wei

Xuanwu Hospital, Capital Medical University

bmusunnyw@163.com+86 13681110149

Outcome results

None listed

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