Evaluation of gynecological and dermatological acceptability of health products using the product at home
- Conditions
- Healthy VolunteersE01.370.600.293
- Registration Number
- RBR-744x3tq
- Lead Sponsor
- Ipclin Instituto de Pesquisa Clínica Integrada Ltda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Women; Age: 18 to 59 years; Phototype: I to IV; Whole skin of the region; Occasional user of category products
Skin marks in the experimental area that interfere in the evaluation of possible
reactions; Pregnant or lactating women; Participants with a history of allergy to the material used in the study; Background of atopy; Use of vaginal cream; Participants with a history of allergy to products in the tested category; Recent gynecological surgeries; Discharges; Immunodeficiency patients; Kidney, heart or liver transplantation;
Active skin pathologies 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, may
compromise the evaluation of the study.
Note: the participants included are instructed not to change their diet, routine
exercises and contraceptive method. Also, not to use products of the same category
of the product tested in the experimental region.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is expected to verify the acceptability of the investigated products in the studied population, after using the products in real use conditions.
- Secondary Outcome Measures
Name Time Method It is expected to guarantee to the community the safety of products.