Development and evaluation of the effectiveness of cosmetics in conjunction with aesthetic procedures

Not Applicable

• Conditions: Skin aging; G13.750

• Registration Number: RBR-2zkkxr3
• Lead Sponsor: Faculdade de Ciências Farmacêuticas da Unicamp

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-02-28
• Study Start: 2023-10-17
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

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

Inclusion Criteria

Women; aged 30 to 65 years; agree with the study conditions; ability to understand and follow the instructions; agree to avoid sun exposure during the study; do not use other cosmetics in the test region throughout the study; be available to attend laboratory sessions on scheduled days; do not wash the test skin region for at least 2 hours before analysis; not having performed aesthetic procedures for at least 3 months

Exclusion Criteria

Lack of cognitive capacity; not understanding the method to be used; be pregnant or breastfeeding; present lesions compatible with active infectious diseases; history of aesthetic plastic surgery in the facial region; history of use of botulinum toxin, fillers or threads; history of recent facial aesthetic treatment, in less than 3 months; have generalized dermatological diseases, such as psoriasis or vitiligo; allergy to any cosmetic product; present systemic diseases with proven effects on the skin; be on continuous treatment with corticosteroids, antihistamines, diuretics, antibiotics, analgesics, anticoagulants, which directly or indirectly affect the skin; carry out immunosuppressive therapy; being treated for endocrine disorders; oophorectomy or hysterectomy; present allergic reactions in the test region during the study; have lesions, wounds, scars, tattoos or piercings in the test region of the skin; presence of metal pins or plates in the craniofacial region; neoplasms, cancer, growing epiphyseal plate and venous thrombosis

Study & Design

• Study Type: Intervention
• Study Design: Not specified