Trials / Completed
CompletedNCT03826017
Efficacy and Safety of Catechin High Contain Greentea Extract on Improvement of Cognitive Function
A 12 Weeks, Randomized, Double-blind, Placebo-controlled Human Trial to Evaluate the Efficacy and Safety of Catechin High Contain Greentea Extract on Improvement of Cognitive Function
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Chonbuk National University Hospital · Academic / Other
- Sex
- All
- Age
- 60 Years
- Healthy volunteers
- Accepted
Summary
This study was the efficacy and safety of Catechin high contain greentea extract on improvement of Cognitive Function
Detailed description
This study was a 12 weeks, randomized, double-blind, placebo-controlled human trial to evaluate. 80 subjects were participated in Catechin high contain greentea extract or placebo group. To evaluate the changes of the evaluation items when Catechin high contain greentea extract was taken 12 weeks compared with placebo.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Catechin high contain greentea extract | Catechin high contain greentea extract 260 mg/day for 12 weeks. |
| DIETARY_SUPPLEMENT | Placebo | Placebo for 12 weeks. |
Timeline
- Start date
- 2018-12-05
- Primary completion
- 2019-10-08
- Completion
- 2019-10-08
- First posted
- 2019-02-01
- Last updated
- 2020-07-16
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03826017. Inclusion in this directory is not an endorsement.