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Clinical Trials/RBR-88ykxm
RBR-88ykxmNot yet recruiting未知

Evaluation of the gynecological and dermatological capacity of health products under normal conditions of use

Ipclin - Pesquisa Clínica Integrada0 sitesStarted: June 5, 2019Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Not yet recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Intervention

Eligibility Criteria

Ages
18Y to 65Y (—)
Sex
Female

Inclusion Criteria

  • Women. Age: 18 to 65 years. Phototype: I to IV. Whole skin of the region. Occasional user of category products

Exclusion Criteria

  • Cutaneous marks in the experimental area that interfere in the evaluation of possible skin reactions (pigmentation disorders, vascular malformations, scarring, increased hairiness, ephelides and nevus in large quantities, sunburns). Pregnant or nursing mothers. 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 cosmetic products of the category tested. Recent gynecological surgeries. Corrections. Immunodeficiency carriers. Renal, cardiac or hepatic transplanted. Active cutaneous 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 opinion of the investigator, could compromise the evaluation of the study

Investigators

Sponsor
Ipclin - Pesquisa Clínica Integrada

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