Trials / Completed
CompletedNCT03274154
Efficacy and Tolerance Evaluation of an Anti-age Food Supplement
Efficacy and Tolerance Evaluation of an Anti-age Food Supplement: a Randomized, Controlled Clinical Study Versus Untreated Group
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 66 (actual)
- Sponsor
- Derming SRL · Academic / Other
- Sex
- Female
- Age
- 35 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
Efficacy and Tolerance Evaluation of an Anti-age Food Supplement: a Randomized, Controlled Clinical Study Versus Untreated Group
Detailed description
Aim of the study was to evaluate the anti-age activity of "Pre-Hyaluron 465 Innēov" a food supplement, composed with a precursor of HA (glucosamine) and an enzymatic co-factor of HA synthesis (manganese), taken for 4 consecutive months by female subjects aged 35-60 years (with preference for subjects over 45 years), with moderate-severe skin aging/photoaging according to a reference photographic scale. The study foresaw the evaluation of the study product activity versus a control group, untreated.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Pre-Hyaluron 465 Innēov | Food supplement consisting og a tablet and a capsule, composed with a precursor of HA (glucosamine) and an enzymatic co-factor of HA synthesis (manganese) |
Timeline
- Start date
- 2016-10-11
- Primary completion
- 2017-03-22
- Completion
- 2017-03-22
- First posted
- 2017-09-06
- Last updated
- 2017-09-06
Source: ClinicalTrials.gov record NCT03274154. Inclusion in this directory is not an endorsement.