Skip to content

Exploratory research on the improvement of brain function in Alzheimer's disease by cervical lymphatic vessel/node-vein anastomosis

Exploratory research on the improvement of brain function in Alzheimer's disease by cervical lymphatic vessel/node-vein anastomosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105306
Enrollment
Unknown
Registered
2025-07-01
Start date
2024-04-30
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Alzheimers disease dementia

Interventions

surgical intervention group:Deep cervical lymphatic vessel/node-venous anastomosis

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The patient or guardian signs the informed consent form; 2. Age 50~80 years old (>= 50 years old, =1 level, <=3 levels);

Exclusion criteria

Exclusion criteria: 1. There are contraindications for MRI, ICG angiography, or PET scan; 2. There are contraindications for lumbar puncture; 3. Severe heart disease or unstable hemodynamics; 4. Severe pulmonary disease, including severe obstructive, restrictive, or mixed ventilatory dysfunction, or Acute inflammation within 3 months; 5. Liver function impairment, with AST or ALT > 3 times the upper limit of normal; 6. Renal dysfunction, with GFR =4 microbleeds in the cerebral lobes; 8. History of cerebral hemorrhage or cerebral infarction with severe neurological dysfunction remaining; 9. Blood diseases, coagulation disorders, abnormal coagulation function; 10. Abnormal thyroid function; 11. Severe stenosis in intracranial or cervical vessels with residual severe neurological dysfunction; 12. Severe hypertension not effectively controlled, with systolic blood pressure >= 180mmHg or diastolic blood pressure >= 110mmHg; 13. The patient has a disease that requires systemic glucocorticoid therapy; 14. Substance abuse (including drugs, narcotics, and alcohol addiction); 15. Severe infectious diseases, including HIV positive and severe infections; 16. Severe mental illness or a potential risk of suicide; 17. Malignant tumor resection within 3 years after surgery; 18. Participated in other interventional clinical trials within the past three months; 19. The physician judged that the compliance was poor, unable to complete or unwilling to cooperate with the regular follow-up after surgery; 20. There are other circumstances that are not suitable for this clinical trial as per the physician's judgment;

Design outcomes

Primary

MeasureTime frame
Changes in scores of clinical symptom related scales;Changes in intracranial pathological protein deposition;

Secondary

MeasureTime frame
Changes in brain structure volume and cerebrospinal lymphatic function index;changes in plasma AD-related biomarker levels;changes in life signs;Cervical Vascular Patency Assessment;Pathological changes in the cervical lymphatic system;changes in CSF AD-related biomarker levels;

Countries

China

Contacts

Public ContactYixin Zhang

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

zhangyixin6688@163.com+86 21 23271699

Outcome results

None listed

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