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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | oréVida™ | 1 capsule 30 mg oréVida™ twice a day (one in the morning, one in the afternoon, so in total 60 mg/day) |
| DIETARY_SUPPLEMENT | oréVida™ | 1 capsule 60 mg oréVida™ twice a day (one in the morning, one in the afternoon, so in total 120mg/day) |
| DIETARY_SUPPLEMENT | oréVida™ | 1 capsule 120 mg oréVida™ in the morning, one placebo capsule in the afternoon (si in total 120 mg/day) |
| DIETARY_SUPPLEMENT | Placebo | 1 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.