Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTCatechin high contain greentea extractCatechin high contain greentea extract 260 mg/day for 12 weeks.
DIETARY_SUPPLEMENTPlaceboPlacebo 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.