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Huperzine A in combination with quercetin in the treatment of Reversible Cognitive Frailty: a randomized controlled trial

Huperzine A in combination with quercetin in the treatment of Reversible Cognitive Frailty: a randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018048
Enrollment
Unknown
Registered
2018-08-28
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

Reversible Cognitive Frailty

Interventions

Experimental group 1:Huperzine A, Quercetin
Experimental group 2:Huperzine A
Experimental group 3:Quercetin
Contro group:Placebo

Sponsors

Huadong hospital, Shanghai medical college, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Reversible cognitive frailty patient: pre-physical frailty and physical frailty (Fried score 2-5); meanwhile, subjective cognitive decline (Spain SCD-Q score 0-7); 2. Aged 60-90 years; 3. MMSE 27-30; 4. Subjects capable of understanding the protocol, complying with its requirements, and attending study visits.

Exclusion criteria

Exclusion criteria: 1. Co-medication with NSAIDs (longterm medication), Gingko- or other natural extracts, other AchE inhibitors; 2. Disability or handicap; visual or hearing impairments in compatible with performance and/or interpretation of neuropsychological tests; 3. Other primary psychiatric/neurologic disorders,such as AD;severe depression or generalized anxiety; acute infection diseaseacute traumatic brain injuries, stroke(< 3 months), autoimmune disease, multiple organ failure, which could be life-threatening in the short term; 4. Missing informed consent; 5. No readiness to save and refer pseudonym personal data; 6. Any condition disturbing or making MRI and other measures impossible; 7. Known allergy of elements of huperzine A, quercetin or placebo; 8. Alcohol or drug abuse; 9. Participation in any clinical trial < 3 months prior to screening or ongoing other clinical trials; 10. Other situation that researchers considered not suite to be included.

Design outcomes

Primary

MeasureTime frame
subjective cognitive decline questionaire;NIA-AA MCI criterian;

Secondary

MeasureTime frame
Fried physical frailty score;Mini-Mental State Examination;The Clinical Dementia Rating;Mild cognitive impairment;The Alzheimer’s Disease Assessment Scale;Pure-tone threshold;Speech audiometry;The Tinnitus Functional Index;Tinnitus Handicap Inventory;Quality of Life-8;Blood biomarkers test;

Countries

China

Contacts

Public ContactYU ZHUOWEI

Huadong hospital,Shanghai medical college, Fudan University

13661717346@163.com+86 13661717346

Outcome results

None listed

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