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OpenTrials
Completed

NCT Number: NCT05779085

Efficacy of a Deep Cleansing Gel Containing 2% Salicylic Acid, 0.2% Zinc Gluconate and 0.05% Lipohydroxy Acid in the Management of Mild to Moderate Facial Acne

A clinical study with 56 healthy subjects (both sexes) aged between 13 to 25 years old. Subjects enrolled had a minimum of 5 inflammatory lesions (papules, nodules and pustules) and 10 non-inflammatory lesions (open and closed comedones), determined by dermatologist. The clinical evaluation considered in oiliness, shininess and global aspect of the skin too. Instrumental assessment of oiliness and shininess was performed, respectively, by Sebumeter and Sebutape.

IThe tested cleanser was used twice daily (morning and evening) during 28 days.

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Key information

Conditions

Acne Vulgaris on the Face

Age range

13 year–26 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Carlos Tortely Hospital

Niterói, 20231-048, Brazil

Who can participate

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

Inclusion criteria

  • subjects aged 13-25 years
  • mild to moderate acne on the face
  • signed informed consent

Exclusion criteria

  • subjects below 13 years and above 26 years
  • severe acne on the face

Treatment and study plan

Dermocosmetic

Other

Use of daily cleanser to treat facial acne

Other names: Cleanser

Primary outcomes

  1. Global lesion count

    Time frame: baseline

    using GEA scale

  2. Global lesion count

    Time frame: Day 28

    using GEA scale

  3. Closed comedones

    Time frame: baseline

    count

  4. Closed comedones

    Time frame: Day 28

    count

  5. papules

    Time frame: baseline

    count

  6. papules

    Time frame: Day 28

    count

  7. skin oiliness

    Time frame: baseline

    instrumental measurement Sebumeter

  8. skin oiliness

    Time frame: Day 28

    instrumental measurement Sebumeter

  9. skin sebutape

    Time frame: baseline

    instrumental measurement Sebumeter

  10. skin sebutape

    Time frame: Day 28

    instrumental measurement Sebumeter

  11. subject satisfaction

    Time frame: Day 28

    questionnaire

Sponsors and collaborators

Lead sponsor

Cosmetique Active International

Industry

Registry information

Official study title

ASSESSMENT OF CLINICAL, INSTRUMENTAL AND NOTICED EFICACY BY SUBJECTS OF A COSMETIC PRODUCT 12.0417.01.090 UNDER NORMAL CONDITIONS OF USE Study With Dermatological Follow-up Including Instrumental Measurements

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Mar 22, 2023
Registry last updated
Mar 22, 2023

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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