Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06727292

Biometrical Evaluation of the Efficacy of a Food Supplement Versus Placebo

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Finzelberg GmbH & Co. KG · Industry
Sex
Female
Age
45 Years – 65 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFood supplementInstant drink in a powder form presented in a sachet to be disolved in a glass of water (200 ml).
DIETARY_SUPPLEMENTPlaceboInstant drink in powder form in a sachet to be disolved in a glass of water (200ml)

Timeline

Start date
2024-10-14
Primary completion
2025-04-01
Completion
2025-05-30
First posted
2024-12-10
Last updated
2024-12-10

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT06727292. Inclusion in this directory is not an endorsement.