Safety evaluation of cosmetic products by gynecologist and dermatologist in normal conditions of use

Not Applicable

• Conditions: Women - Other specified noninflammatory disorders of vagina; M01.975

• Registration Number: RBR-5j38t9
• Lead Sponsor: Ipclin - Pesquisa Clínica Integrada

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-07-11
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Female. Age 18 to 65 years. Phototype I to IV. Intact skin in the test area. Occasional user of the category products

Exclusion Criteria

Cutaneous marks in the experimental area that interfere with the evaluation of possible skin reactions (pigmentation disorders, vascular malformations, scars, increased hairiness, ephelides and nevus in large quantities, sunburn). Pregnant women or infants. Subjects with a history of allergy to the material used in the study. History of atopy. Use of vaginal cream. Subjects with a history of allergy to cosmetic products of the tested category. Recent gynecological surgeries. Vaginal discharge. Immunodeficiency carriers. Renal, cardiac or hepatic transplanted. Active cutaneous pathologies that may interfere with the study (vitiligo, psoriasis, lupus, atopic dermatitis). Topical use of corticosteroids in the experimental area up to 8 days before the start of the study.

Study & Design

• Study Type: Intervention
• Study Design: Not specified