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Effect of cervical lymphaticovenous anastomosis and cervical lymph node to vein anastomosis for the patient with intracranial lymphatic circulation disorder

Effect of cervical lymphaticovenous anastomosis and cervical lymph node to vein anastomosis for the patient with intracranial lymphatic circulation disorder

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CRIS
Registry ID
KCT0010302
Enrollment
114
Registered
2025-03-14
Start date
2025-02-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

Procedure/Surgery : Among the patients evaluated with a GDS score of 3-5 for neurological treatment at Asan Medical Center in Seoul between December 31, 2025, the study was conducted on 114 patients (

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Between December 31, 2025, from the IRB approval date to December 31, 2025, among patients with intracranial lymphoma circulation disorders evaluated with a GDS score of 3-5, we plan to take amyloid PET CT and conduct a study on Alzheimer's disease patients whose accumulation of amyloid due to lymphoid circulation disorders was objectively confirmed.

Exclusion criteria

Exclusion criteria: - Patients under 45 years of age and over 80 years of age are excluded. -Except when follow-up observation is not possible for more than 12 months. -Patients with vascular dementia are excluded. -Patients with organic brain disease are excluded. -Patients with indocyanine green (ICG) hypersensitivity are excluded. -Except for cases where general health is not controlled due to a serious medical condition. -Patients with a history of past surgery in the neck are excluded. -Except if you do not want to or have not filled out the consent form. -Other than the above matters, cases where it is deemed difficult to conduct clinical trials at the judgment of the clinical trial director shall be excluded

Design outcomes

Primary

MeasureTime frame
Cognitive function evaluation

Secondary

MeasureTime frame
postoperative side effects

Countries

Korea, Republic of

Contacts

Public Contactjuhee hwang

Asan Medical Center

juheex301@gmail.com+82-2-2045-4291

Outcome results

None listed

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