Assessment of Gynecological and Dermatological Acceptability of Health Product under Normal Conditions of Use
- Conditions
- qualified volunteerswomenM01.774.500M01.975
- Registration Number
- RBR-6fb473
- Lead Sponsor
- abterapi Laboratório de produtos naturais EIRELI EPP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Female
- Target Recruitment
- Not specified
Women; Age 18 to 65 years old; Phototype I to IV
Whole skin of the region; Occasional user of category products
Skin markings in the experimental area that interfere with the evaluation of possible reactions
Pregnant or lactating women;
Participants with a history of allergy to the material used in the study;
History of atopy;
Use of vaginal cream;
Participants with a history of allergy to products of the tested category;
Recent gynecological surgeries;
Discharge;
Carriers of immunodeficiencies;
Kidney, cardiac or liver transplantation;
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 opinion of the investigator, may compromise the evaluation of the study.
Note: Participants included are advised not to change their diet, exercise routine and contraceptive method. Also, not to use products from the same category as the product tested in the experimental region.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method