Recruitment of volunteers.
To assess the comedogenicity of a skincare product, laboratories call upon a score of volunteers, aged between 18 to 65 years, who have no history of intolerance or allergy to a cosmetic product. Moreover, certain individuals are unable to participate in comedogenicity studies. These include pregnant women, people with a skin condition (acne, eczema, psoriasis, vitiligo...), those undergoing certain types of medication treatment recently (for example: change or cessation of 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 a period of 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 moisturising cream, volunteers will be asked to apply it to their facial skin after it has been thoroughly 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 alter their other hygiene and cosmetic habits.
After the study.
At the end of the four weeks, the volunteers return to the study centre 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.