Recruitment of volunteers.
To assess the comedogenicity of a skincare product, laboratories rely on a group of about twenty volunteers, aged between 18 and 65 years, who have no history of intolerance or allergy to any cosmetic product. However, certain individuals are not eligible to participate in comedogenicity studies. These include pregnant women, individuals with a skin condition (acne, eczema, psoriasis, vitiligo...), those who have recently started certain types of medication (for example, those who have changed or stopped hormonal treatment less than 5 weeks ago), and individuals with significant body hair, freckles, moles , or a tattoo in the area of the experiment.
During the study.
For 4 weeks, participants are required to apply the tested cosmetic product daily, adhering to specific conditions set by the laboratory. For instance, in the case of a moisturizing cream, volunteers will be asked to apply it to their facial skin that has been previously cleaned and dried. After each use, participants are required to fill out an observation document detailing the condition of their skin and their sensations upon application (feelings of warmth, redness, itching, tingling, tightness...). Moreover, during the study period, the use of a product similar to the one being tested is not permitted. Volunteers are also asked not to change their other hygiene and cosmetic habits.
After the study.
At the end of the four weeks, the volunteers return to the study center where a clinical examination is conducted. The skin lesions are counted (comedones and microcysts) and the participant observation document is reviewed. The data is then processed electronically. The appearance or non-appearance of skin lesions during the study allows conclusions to be drawn about the occlusive potential of the product tested.