Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTPre-Hyaluron 465 InnēovFood 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.