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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Placebo supplement | Cellulose |
| DIETARY_SUPPLEMENT | Citicoline supplement | Cognizin ® |
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.