Clinical Trials Directory

Trials / Completed

CompletedNCT06047899

Influence of Luteolin for Two Weeks on Memory in Healthy Subjects

Influence of the Dietary Supplement Luteolin for Two Weeks on Memory in Healthy Subjects

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Prof. Dominique de Quervain, MD · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to learn about the effect of the dietary supplement luteolin in healthy people. The main question it aims to answer is: Does luteolin have an influence on memory functions? Participants will go trough two treatment phases. In one phase they will take 250mg luteolin twice daily for two weeks. In the other phase they will take a placebo twice daily for two weeks. A placebo is a look-alike substance that contains no active drug. At the start and end of teach treatment phase, participants will undergo different memory testing exercises in our research facility.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLuteolinLuteolin extracted from Chrysanthemum Ramat 98% HPLC by Scyherb® food grade certified according to Safe Quality Foods (SQF) - Level 3 Comprehensive Food Safety and Quality Management System Certification by the Safe Quality Food Institute (SQFI).
OTHERPlacebomannitol formulated for oral administration (capsules)

Timeline

Start date
2023-11-28
Primary completion
2024-05-02
Completion
2024-05-02
First posted
2023-09-21
Last updated
2024-05-09

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT06047899. Inclusion in this directory is not an endorsement.