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Randomized controlled clinical trial of deep cervical lymphangiovenous anastomosis in the treatment of Alzheimer's disease

Randomized controlled clinical trial of deep cervical lymphangiovenous anastomosis in the treatment of Alzheimer's disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094603
Enrollment
Unknown
Registered
2024-12-25
Start date
2024-08-29
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Alzheimer's disease

Interventions

Experimental group:Bilateral jugular deep lymphatic venous anastomosis was performed.
control group:Non operative treatment (conservative treatment).

Sponsors

The First People's Hospital of Zunyi City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Meet the above clinical diagnostic criteria and symptom staging criteria for Alzheimer's disease; (2) Subject age> 50 years old; (3) The course of the disease > 6 months; (4) The comprehensive score of the Clinical Dementia Rating Scale (CDR) is 2 or 3 points, that is, moderate dementia or severe dementia; (5) The Mini-Mental State Examination (MMSE) score is 10~15 points, accompanied by dementia mental and behavioural symptoms (BPSD) (6) No history of mental illness and epilepsy in the past, and no serious diseases of other organs, i.e., systems: (7) Patients and their families have understood the purpose, significance, expected effects and potential risks of this study in detail and voluntarily joined the trial, and signed the relevant informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with non-AD or mild AD; (2) Those who suffer from other mental illnesses or cognitive dysfunction due to depression, Parkinson's, cerebral infarction and other diseases; (3) Combined tumours, cardiovascular and cerebrovascular diseases, bleeding diseases, severe liver and kidney insufficiency, etc.; (4) Those who have received relevant treatment within 1 month of participating in this study: (5) The use of multinepezil, mannute sodium capsule (GV-971), and olanzapine within 3 months of participating in this study to affect cognitive and psychiatric symptoms; (6) Those who cannot tolerate cervical lymph node-venous anastomosis.

Design outcomes

Primary

MeasureTime frame
Mini Mental State Examination (MMSE) score;Alzheimer's Disease Assessment Scale Cognitive Scale (ADAS Cog) score;Activities of Daily Living Scale (ADL) score;

Secondary

MeasureTime frame
Aß protein;Tau protein;inflammatory factors;

Countries

China

Contacts

Public ContactFu Xiaohong

The First People's Hospital of Zunyi City

136166618@qq.com+86 180 8964 0215

Outcome results

None listed

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