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Ensaios Clínicos (somente visualização)
Listagem completa dos ensaios clínicos importados do XML ICTRP.
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Id:
393
Trial ID:
RBR-82y4dz
Public Title:
Evaluation of the skin firmness and elasticity
Scientific Title:
Evaluation of the skin firmness and elasticity
Scientific Title Native:
None
Recruitment Status:
Data analysis completed
Study Type:
Intervention
Study Design:
4, single-arm-study, single-blind
Study Phase:
4
Allocation:
None
Masking:
None
Purpose:
None
Date Registration:
2015-02-18
Date Enrolment:
2014-05-15
Last Refreshed:
None
Source Register:
None
Primary Sponsor:
KOSMOSCIENCE CIENCIA E TECNOLOGIA COSM IMP EXP LTDA
Secondary Sponsors:
Herbarium Laboratório Botânico Ltda
Web Address:
https://ensaiosclinicos.gov.br/rg/RBR-82y4dz
Target Size:
None
Inclusion Criteria:
Female volunteers, aged between 18 and 60 years, with skin phototype I to IV and intact skin in the region of the test; signs of sagging in the area evaluated; good physical condition and mental health; agreement not to use any topical products on the arms between the 48 h period before the day of the beginning of the study until the end of this; signing the Informed Consent Form ICF.
Exclusion Criteria:
Skin marks in the experimental area that interfere with evaluation of possible skin reactions, pigmentation disorders , vascular malformations , scars , increased hairiness , freckles and warts aplenty, sunburn ; dermatoses active local or widespread , that may interfere with results of the study . Pregnant or lactating ; a history of allergic reactions , irritation or discomfort to intense feelings of topical products : cosmetics or medicines ; history of atopy ; intense sun exposure or tanning session up to 15 days before the initial evaluation or during the study prediction of intense sun exposure during the study ; body dermatological aesthetic treatment or up to 03 weeks before selection, such as : mesotherapy , carboxiterapia and body peels. Use of the following medications topical or systemic use : immunosuppressants , antihistamines , NSAIDs and corticosteroids to 2 weeks prior to or during the study period ; treatment with Vitamin A acid and / or its derivatives orally or topically for 1 month prior to study initiation . Be participating in another study or have participated in another study with cosmetic until a week before the study inclusion ; ingestion of nutritional supplements that can influence the results of the study ; any condition which , in the opinion of the investigator , may compromise the evaluation of the study .
Health Conditions:
None
Interventions Summary:
None
Contacts Summary:
None
Results:
None
Countries:
Updated On:
2026-06-01 05:16:46