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Biometrical Evaluation of the Efficacy of a Food Supplement Versus Placebo

NCT06727292 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2024-12-10

No results posted yet for this study

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

  • Skin Aging
  • Hair Condition
  • Skin Condition

Interventions

DIETARY_SUPPLEMENT

Food supplement

Instant drink in a powder form presented in a sachet to be disolved in a glass of water (200 ml).

DIETARY_SUPPLEMENT

Placebo

Instant drink in powder form in a sachet to be disolved in a glass of water (200ml)

Sponsors & Collaborators

  • Eurofins

    collaborator INDUSTRY

  • Eurofins Dermscan Pharmascan

    collaborator INDUSTRY

  • Finzelberg GmbH & Co. KG

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-14
Primary Completion
2025-04-01
Completion
2025-05-30

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06727292 on ClinicalTrials.gov