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This is a multi-center, randomized, double-blind, placebo-controlled, Phase IV Trial to evaluate the efficacy and safety of Choline Alfoscerate compared to placebo in Mild Cognitive Impairment Patients with Cerebrovascular Disease
Full description
Subject will be randomised in a 1:1 ratio to receive either Choline Alfoscerate or it's placebo. Investigational Product(IP, Choline Alfoscerate or it's placebo) will be administered 3 times a day per oral during the treatment
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Allocation
Interventional model
Masking
418 participants in 2 patient groups, including a placebo group
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Central trial contact
Sun U Kwon, MD, PhD
Data sourced from clinicaltrials.gov
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