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A Prospective,Multicenter Cohort Study of Cervical Deep Lymphovenous Anastomosis for the Treatment of Alzheimer's Disease

A Prospective,Multicenter Cohort Study of Cervical Deep Lymphovenous Anastomosis for the Treatment of Alzheimer's Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097585
Enrollment
Unknown
Registered
2025-02-21
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Alzheimers disease

Interventions

Group A Intervention Group:Deep cervical lymphatic-venous anastomosis
Group B Control group:Non-surgical treatment

Sponsors

Kunming Sanbo Brain Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Clinical diagnosis consistent with Alzheimer's disease-related cognitive impairment or Alzheimer's disease with dementia; (2) Age between 50 and 85 years (inclusive), regardless of gender; (3) Moderate to severe cognitive decline (MMES <= 20 points or MoCA < 20 points); (4) Patients with Alzheimer's disease (AD) who are unable or unwilling to be treated by other methods; (5) Disease duration of 6 months or longer, with conservative treatment for 3 months or longer; (6) Ability to complete the cognitive and other tests specified in the project protocol as required; (7) Presence of a stable and reliable caregiver, or frequent contact with a caregiver (at least 4 days per week, for more than 2 hours each day), and the caregiver or immediate family member is willing to sign the informed consent form to assist the participant in this study. The caregiver is required to accompany the participant to the study visits and have sufficient interaction and communication with the participant to provide the necessary information for the study.

Exclusion criteria

Exclusion criteria: (1) Presence of unassessed or untreated moderate to severe hydrocephalus, brain tumors, and other serious cranial diseases; (2) History of severe traumatic brain injury, large cerebral infarction, craniotomy for cerebral hemorrhage, and severe intracranial infection; (3) Presence of uncontrolled systemic infection or surgical site infection; (4) Coexisting malignant tumors of the cranial and peripheral regions with a life expectancy of less than one year; (5) Hematological diseases and coagulation mechanism disorders (hypercoagulable or hypocoagulable states); (6) Other conditions that cannot tolerate anesthesia and surgery.

Design outcomes

Primary

MeasureTime frame
Intelligence (MMSE, MoCA and ADL scales );ß amyloid;Tau;

Countries

China

Contacts

Public ContactHaoRan Wang

Kunming Sanbo Brain Hospital

whr0517@126.com+86 158 1015 2329

Outcome results

None listed

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