Clinical Study to Assess Anticellulite Efficacy

Not Applicable

• Conditions: cellulite; C23.888.885.281

• Registration Number: RBR-2j26pk
• Lead Sponsor: Malwee Malhas Ltda,

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-04-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Age from 18 to 45 years; Women; Healthy participants (evaluated by the dermatologist); Phototypes I to IV (according to the Fitzpatrick classification), due to the study of acceptability and the
possibility of quickly detecting skin reactions with this scale; Presence of cellulite in the experimental region (buttocks and thighs); Presence of grade I, II, III and IV cellulite; Participants who accept not to change the normal daily routine of their cosmetic habits, except for the use of topical products with activity similar to the test product during the entire study, these do not
must be used; The Informed Consent Form (ICF) has been clarified and signed; Participants who want to participate in the study without financial profit. They will be reimbursed for expenses related to the test, such as transportation and food, among others; Participants who have not participated in similar studies for at least 2 months prior
to study; Regular / occasional users of cosmetic products similar to the product under investigation; Participants who declared they were not at risk of pregnancy during the survey period

Exclusion Criteria

Allergy to the tested product category; Pregnancy or lactation; Immunodeficiencies; Active atopic dermatitis; Kidney, heart or liver transplantation; Use of the following medications: corticosteroids, antihistamines, immunosuppressants, retinoids, anti-inflammatories; Any condition that may interfere with the evaluations according to the Investigator of the study; Participants who refuse to participate in the study in question.
Note: the participants included are instructed not to change their diet, cosmetic and hygiene habits, exercise routine and contraceptive method. Also, not to use products of the same product category
tested in the experimental region

Study & Design

• Study Type: Observational
• Study Design: Not specified