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Completed

NCT Number: NCT06956625

Cleansing Efficacy of Cosmetic Product

The aim of this study is to investigate the cleansing effect of one cosmetic product containing Mitopure against a particular matter model pollutant in comparison to an untreated control.

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Key information

Conditions

Healthy Skin

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

SGS proderm GmbH

Schenefeld, Germany

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent to participate in the study
  • Willingness to actively participate in the study and to come to the scheduled visits
  • Female and/or male
  • From 18 to 70 years of age
  • Healthy skin in the test area
  • Skin type on Fitzpatrick scale: I, II or III

Exclusion criteria

  • Female subjects: Pregnancy or lactation
  • Drug addicts, alcoholics
  • AIDS, HIV-positive or infectious hepatitis
  • Conditions which exclude a participation or might influence the test reaction/evaluation
  • Participation or being in the waiting period after participation in cosmetic and/or pharmaceutical studies pertaining to the test area
  • Cancer not being diagnosed as cured and requiring chemotherapy, irradiation and/or hormonal treatment within the last 2 years
  • Active skin disease at the test area
  • Wounds, moles, tattoos, scars, irritated skin, excessive hair growth, etc. at the test area that could influence the investigation
  • Any topical medication at the test area within the last 4 weeks prior to the start of the study and during the study
  • Documented allergies to cosmetic products and/or ingredients

Treatment and study plan

Topical cosmetic cleanser

Other

After applying the model pollutant, the test area will be topically cleaned with the active cosmetic cleanser with Mitopure.

Topical tap water

Other

After applying the model pollutant, the test area will be topically cleaned with tap water (control).

Primary outcomes

  1. Luminosity (L)

    Time frame: Before pollutant application (t0), immediately after evaporation of the applied pollutant (t1), and 20 minutes after product rinse-off (t2)

    Luminosity in test area assessed by HiRIS (High Resolution Imaging System) image analysis will be used to quantify cleaning efficacy.

Sponsors and collaborators

Lead sponsor

Amazentis SA

Industry

Collaborators

  • SGS proderm GmbH

Registry information

Official study title

Cleansing Efficacy of Cosmetic Products - Particular Matter Model

Acronym: Cleanser

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 4, 2025
Registry last updated
Jun 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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