Trials / Completed
CompletedNCT05537350
A Clinical Study to Evaluate the Efficacy and Consumer Perception of Lumenato
A 12 Weeks of Clinical Study to Evaluate the Efficacy and Consumer Perception of Different Skin Attributes Following Supplementation of an Oral Supplement- Lumenato
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 66 (actual)
- Sponsor
- LycoRed Ltd. · Industry
- Sex
- Female
- Age
- 35 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
Subjects will be enrolled in this clinical study to assess the efficacy of an oral supplement to change the characteristics of facial skin after 4 and 12 weeks of use and obtain consumer perception of the test product through the use of questionnaires. Study evaluations will include a comprehensive metabolic panel, Cutometer measurements, Canfield's VISIA-CR images, VapoMeter Measurements, and Consumer perception questionnaires.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Lumenato | Supplementation of 12 weeks |
Timeline
- Start date
- 2022-01-04
- Primary completion
- 2022-06-01
- Completion
- 2022-08-31
- First posted
- 2022-09-13
- Last updated
- 2022-09-13
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05537350. Inclusion in this directory is not an endorsement.