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Clinical Trials/RBR-2z27nc9
RBR-2z27nc9
Not yet recruiting
Not Applicable

A clinical trial to evaluate the safety of the investigational product denture fixing cream without flavor , evaluating the acceptability in the oral mucosa and perceived efficacy under normal conditions of use

Kosmoscience Ciência e Tecnologia Cosmética Limitada0 sitesApril 12, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Edentulous arcade
Sponsor
Kosmoscience Ciência e Tecnologia Cosmética Limitada
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 12, 2022
End Date
May 16, 2022
Last Updated
2 years ago
Study Type
Observational

Investigators

Sponsor
Kosmoscience Ciência e Tecnologia Cosmética Limitada

Eligibility Criteria

Inclusion Criteria

  • Age range between 18 and 60 years. Female and male. Phototype (Fitzpatrick): I to VI. Being a user of removable dental prostheses (dentures). Be a user of products of the same category. Agree on procedures and requirements during study use: study time (after 21 days) laboratory to perform investigational product home study procedures, change the product study diary, do not change the study product study diary. Agree to perform facial aesthetic dermatological treatments until the end of the study (21 days), such as: peelings, laser, fillers, use of any unusual suitable products

Exclusion Criteria

  • Pregnant or lactating women. Participant who belongs to the risk group for COVID\-19, that is, with cardiovascular, renal and chronic respiratory problems, immunosuppressed or other conditions that the doctor judges as belonging to the risk group. Presence of dermatoses, active skin lesions (local and/or disseminated) or irritation in the mouth region (internal or external). Expected vaccination during the study or up to 3 weeks before the study. History of oral pathologies. Use of non\-steroidal anti\-inflammatory drugs, corticosteroids, antihistamines, photosensitizers or immunosuppressants up to 2 weeks before the study. Be participating in another study in the same application region. History of non\-adherence or unwillingness to adhere to the study protocol. Being undergoing dental treatment. Not taking vitamin A or derivatives. Any condition that, in the opinion of the researcher, could compromise the study. (To describe)

Outcomes

Primary Outcomes

Not specified

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