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Neck surgery may help clear Alzheimer's toxins from the brain

NCT ID NCT07669272

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a one-time microsurgery that connects lymphatic vessels in the neck to veins, aiming to improve drainage of waste proteins from the brain. Fifty-nine people with severe Alzheimer's will receive the surgery plus standard medication. Researchers will measure changes in cognitive function and brain scans over 12 months to see if the procedure is safe and effective.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Deep Cervical Lymphovenous Anastomosis (a microsurgical procedure to connect lymphatic vessels to neck veins)
What this could lead to
If successful, this could offer a new way to slow cognitive decline in severe Alzheimer's by helping the brain clear toxic proteins.
What could go wrong
This is a very early, small study with no control group, so results may not be reliable. Surgery carries risks like infection or anesthesia complications, and the benefit is unproven.

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

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

About 59 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Sep 2029

An estimate. End dates often move.

Lead sponsor

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

50 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Meet the 2011 NIA-AA clinical diagnostic criteria for probable Alzheimer's disease dementia and the 2018 NIA-AA research framework biomarker criteria for AD. * Aged 50 to 80 years (inclusive) at the time of signing informed consent. * Severe cognitive dysfunction: Mini-Mental State Examination (MMSE) score \< 10 points. * Progressive cognitive deterioration for more than 6 months reported by patient or caregiver. * No clinical improvement after more than 6 months of standardized drug treatment. * Have a designated study companion who signs informed consent, contacts the patient at least 10 hours per week and accompanies study visits. * Able to complete scale assessments and examinations independently or with companion assistance. * Voluntarily comply with study procedures, examinations and surgical treatment. * Patient or legal representative can sign written informed consent and abide by trial requirements. * Patients and families are informed of study purpose, expected efficacy and potential risks, and voluntarily provide biological samples and participate in the study. Exclusion Criteria: * Severe central nervous system diseases (other than AD) that affect cognitive function or study compliance. * Severe/unstable systemic diseases (cardiovascular, hepatic, renal, respiratory, endocrine, hematological, psychiatric diseases); life expectancy less than 24 months. * Surgical contraindications: severe coagulation disorders, severe -cardiopulmonary diseases (myocardial infarction/respiratory failure within recent 30 days); severe liver damage (ALT/AST \> 3 times upper limit of normal); severe renal insufficiency (eGFR \< 30ml/min). * Severe primary mental disorders (other than AD) that interfere with efficacy evaluation and cognitive assessment. * History of intracranial hemorrhage or craniocerebral trauma within recent 1 year. * Alcohol or drug abuse/dependence within recent 1 year. * Allergy to indocyanine green, gadolinium contrast agent, 18F-florbetapir or 18F-flortaucipir. * Contraindications for PET examination. * Other conditions judged by investigators unsuitable for enrollment.

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • The First Affiliated Hospital of Army Medical University (Southwest Hospital)

    Chongqing, Chongqing Municipality, 400038, China

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