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Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07854327). This is a study registration, not published results. Lead sponsor: University of Siena. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 5 participants (ESTIMATED). Conditions: Alzheimer, Alzheimer Dementia (AD). Interventions: PROCEDURE: Cervical lymphovenous anastomosis (LVA); PROCEDURE: Cervical lymphovenous anastomosis (LVA). Primary outcome measures: Change from baseline in plasma amyloid-beta concentrations , Baseline, 1 month, and 6 months after LVA; Change from baseline in plasma phosphorylated tau concentrations , Baseline, 1 month, and 6 months after LVA; Change from baseline in plasma NfL and GFAP concentrations , Baseline, 1 month, and 6 months after LVA. Brief summary: Alzheimer's disease (AD) is a progressive neurodegenerative disorder associated with the accumulation of abnormal proteins, including amyloid-beta and tau, in the brain. Recent evidence suggests that the glymphatic and meningeal lymphatic systems, which contribute to the removal of waste products from the brain, may play a role in AD. In particular, impaired drainage through the deep cervical lymphatic system may contribute to the accumulation of disease-related proteins. The LymphDAD study is a prospective, single-center pilot study designed to explore whether surgically improving cervical lymphatic drainage may be associated with changes in biological markers, brain imaging, and cognitive and clinical measures in selected patients with AD who are not eligible for currently available disease-modifying treatments. Five participants with AD will undergo a minimally invasive microsurgical procedure called lymphovenous anastomosis (LVA), in which small cervical lymphatic vessels are connected to nearby small veins to facilitate lymphatic drainage. During the procedure, a small sample of lymphatic fluid will also be collected for exploratory analysis of amyloid-beta and tau proteins. Participants will undergo clinical and neuropsychological assessments, blood sampling, magnetic resonance imaging (MRI), and amyloid positron emission tomography (PET) before the procedure and during follow-up. Follow-up assessments will be performed at 1, 3, 6, and 12 months after surgery. The study is exploratory and is not designed to demonstrate a definitive clinical benefit. Its primary purpose is to obtain preliminary information on the feasibility, safety, and possible biological and clinical effects of cervical LVA in AD, which may support the design of future controlled studies.