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Clinical Trial Summary

A pre-post study will be conducted to assess whether treatment with LXB, nVNS or a combination of both interventions can enhance the clearance of Aβ in patients with CAA. A total of 60 subjects, 30 with sCAA and 30 with D-CAA, will be randomly assigned to receive LXB, or both interventions. The primary outcome measure will be the morning levels of Aβ40 and Aβ42 in cerebrospinal fluid (CSF) before and after the intervention. The investigators will assess disease progression with (non-)haemorrhagic imaging markers on 7-Tesla Magnetic Resonance Imaging (7-T MRI) as a secondary outcome. Additionally, the activity of the glymphatic system by means of fluid dynamics will be assessed using 7-T MRI.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06421532
Study type Interventional
Source Leiden University Medical Center
Contact Sanne Schriemer, MD
Phone +31715261825
Email clear-brain@lumc.nl
Status Not yet recruiting
Phase Phase 2
Start date June 1, 2024
Completion date August 1, 2026

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