Neck surgery may help clear brain waste in Alzheimer's – new trial underway
NCT ID NCT07328386
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a neck surgery (lymphaticovenous anastomosis) to improve drainage of fluid from the brain in people with Alzheimer's disease. About 114 participants will either receive surgery plus standard medication or medication alone. Researchers will track changes in memory and thinking over two years to see if the surgery slows cognitive decline.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 114 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged 19 years or older who are diagnosed with intracranial lymphatic circulation disorder based on neurological evaluation. * Global Deterioration Scale (GDS) score between 3 and 5 at screening. * Diagnosis of Alzheimer's disease confirmed by amyloid PET-CT or CSF amyloid testing, showing amyloid accumulation associated with lymphatic circulation disorder. * Able to provide written informed consent to participate in the study voluntarily. Exclusion Criteria: * Unable to undergo follow-up evaluation for at least 12 months after surgery. * Diagnosed with vascular dementia. * Presence of structural brain disease other than intracranial lymphatic circulation disorder. * Known hypersensitivity to indocyanine green (ICG). * Uncontrolled systemic medical conditions such as severe cardiopulmonary, renal, hepatic, or endocrine disorders. * History of previous neck surgery. * Refusal to participate or failure to provide informed consent. * Determined by the principal investigator to be unsuitable for participation due to any other clinical reason.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Asan Medical Center
RECRUITINGSeoul, South Korea
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