Biometrical Evaluation of the Efficacy of a Food Supplement Versus Placebo
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age45-65
SponsorFinzelberg GmbH & Co. KG
About this trial
The purpose of this clinical trial is to evaluate whether nutritional supplementation over a 2-month period improves skin physiological parameters. This is a national, single-center, double-blind, randomized pilot study.
The study will be conducted using a supplement and a placebo, the safety of which has been assured by the sponsor.
Participants will:
* Take a food supplement or a placebo once daily for 2 months * Visit the study center at beginning, after 28 days and after 56 days of supplementation. * Keep a diary of their skin status and tolerability
The secondary objective is to evaluate product characteristics and performance during normal use in healthy subjects.
Eligibility criteria
Qualifiers
Phototype: I to IV;
Subjects with normal to dry skin;
Subjects with healthy skin on the study area;
Non-smokers;
Disqualifiers
For women: pregnant or nursing woman or woman planning to get pregnant during the study;
Cutaneous pathology on the study zone (eczema, etc.);
Subject with make-up on the day of the visit at the laboratory;
change in anti-wrinkle, smoothing and/or firming topical products within previous week on the studied zones,
Trial design
Treatments tested in this trial
- Food supplement
- Placebo
Treatment groups
66 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov