Healthy Volunteers
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women; age: 18 to 59 years; phototype: I to IV; whole skin of the region; occasional user of category products
Exclusion criteria
Exclusion criteria: Skin marks in the experimental area that interfere with the assessment of possible reactions; Pregnant or lactating women; Participants with a history of allergy to the material used in the study; Atopy history; Use of vaginal cream; Participants with a history of allergy to products from the tested category; Recent gynecological surgeries; Discharges; Immunodeficiency patients; Kidney, cardiac or liver transplants; Active skin conditions that may interfere with the study (vitiligo, psoriasis, lupus, atopic dermatitis); Topical use with corticosteroids in the experimental area up to 8 days before the start of the study.; Any condition not mentioned above that, in the investigator's opinion, could compromise the study evaluation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to verify the acceptability of the investigational product, an intimate lubricant, in the studied population, after using the products in real conditions of use, through dermatological and gynecological medical evaluation of clinical signs and feelings of discomfort, based on the finding of that none of the participants presented discomfort or clinical signs, considering the product as gynecologically and dermatologically tested. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to guarantee the safety of the product, an intimate lubricant, to the end users, based on the observation that none of the participants presented discomfort or clinical signs. | — |
Countries
Brazil