Clinical Trials Directory

Trials / Completed

CompletedNCT04967157

Cognitive Effects of Citicoline on Attention in Healthy Mean and Women

A Randomized, Parallel, Double-Blind, Placebo-Controlled Study to Assess the Cognitive Effects of a Citicoline Supplement (Cognizin®) on Attention in Healthy Men and Women

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
148 (actual)
Sponsor
Kirin Holdings Company, Limited · Industry
Sex
All
Age
35 Years – 75 Years
Healthy volunteers
Accepted

Summary

The objective of this trial is to determine the effects of citicoline on cognitive performance for attention in healrhy Men and Women compared to a placebo.

Detailed description

This study is a 12-week, randomized, double-blind, placebo-controlled trial of citicoline in healthy men and women. Cognitive assessments will be performed to determine whether citicoline administration improves attention, compared to placebo administration. \*\*Note: This note is to inform you that the Unique Protocol ID BIO-2104 was unintentionally combined with another Unique Protocol ID, K5-24-01-T0060, resulting in history records that should not be considered as part of the BIO-2104's timeline. This explanation has been added per PRS instructions to ensure compliance and maintain data integrity in alignment with the protocol.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPlacebo supplementCellulose
DIETARY_SUPPLEMENTCiticoline supplementCognizin ®

Timeline

Start date
2021-09-08
Primary completion
2022-08-31
Completion
2022-08-31
First posted
2021-07-19
Last updated
2025-04-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04967157. Inclusion in this directory is not an endorsement.