Clinical Trials Directory

Trials / Completed

CompletedNCT01143194

A Randomized, Placebo-Controlled, Double-Blind, Crossover Study to Evaluate the Effects of Three Doses of the Dietary Supplement oréVida™ on Alertness, Attention and Concentration in Healthy Men and Women

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
44 (actual)
Sponsor
dsm-firmenich Switzerland AG · Industry
Sex
All
Age
35 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate the effects of the dietary supplement oréVida™ (active ingredient on the basis of a culinary herb)administered twice daily in an acute study on an improvement in vigilance, attention, concentration, memory and mood in 45 healthy men and pre-menopausal women, aged 35-50 years, inclusive. oréVida™ is considered a dietary supplement, and therefore it is not an approved drug by the Food and Drug Administration (FDA). It is regulated like a food. The U.S. Food and Drug Administration does not strictly regulate herbs and dietary supplements. We do not claim that this supplement is meant to treat any ailment.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENToréVida™1 capsule 30 mg oréVida™ twice a day (one in the morning, one in the afternoon, so in total 60 mg/day)
DIETARY_SUPPLEMENToréVida™1 capsule 60 mg oréVida™ twice a day (one in the morning, one in the afternoon, so in total 120mg/day)
DIETARY_SUPPLEMENToréVida™1 capsule 120 mg oréVida™ in the morning, one placebo capsule in the afternoon (si in total 120 mg/day)
DIETARY_SUPPLEMENTPlacebo1 capsule of placebo twice a day

Timeline

Start date
2010-03-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2010-06-14
Last updated
2011-06-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01143194. Inclusion in this directory is not an endorsement.