RBR-6hnmxv
Active, not recruiting
未知
Dermatological assessment of primary dermal irritability accumulated and sensitization.
Ipclin - Pesquisa Clínica Integrada0 sitesOctober 10, 2019
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Wounds and injuries
- Sponsor
- Ipclin - Pesquisa Clínica Integrada
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Full skin in the study region (back); Age 18 to 65 years; Gender; male or female, Participants with phototypes I; II; III and IV (according to Fitzpatrick's classification); Absence of irritation allergy history to the material used in the study; Have signed the Term of Free and Informed Consent (TCLE); Participants who want to participate in the study without financial gain. They will only be reimbursed for transportation and food expenses.
Exclusion Criteria
- •Participants who refuse to participate in the study in question; Skin 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; sunburn); Dermatoses (local and disseminated) that could interfere with the results of the study; Pregnant women or infants; History of allergic reactions; irritation or intense discomfort feelings to topical products; for health and medicines; Volunteers with a history of allergy to the material used in the study; History of atopy; History of conditions aggravated or triggered by ultraviolet radiation; Immunodeficiency carriers; Kidney; cardiac or hepatic transplanted patients; Intense sun exposure or tanning session up to 15 days prior to initial evaluation; Forecast of intense sun exposure or session of bron during the course of the study; Forecast of bathing; pool or sauna during the study; Participants practicing aquatic sports;
- •Use of the following topical systemic medicinal products; immunosuppressive; antihistaminic; non\-hormonal anti\-inflammatory drugs; and corticosteroids up to two weeks prior to selection; Treatment with acid vitamin A and or its derivatives via oral or topical use up to 01 month before start of the study; Vaccination prediction during the study or up to 03 weeks before the study; Any condition not mentioned above that in the opinion of the investigator could compromise the evaluation of the study.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
24 hours patch test to verify the Primary irritation of a research productCTRI/2014/02/004427Stempeutics Research Pvt Ltd24
Not yet recruiting
Not Applicable
Health Product Irritability and Sensitization Assessment through Contact TestArtificial toothE06.780.346.875RBR-587ptdIpclin - Pesquisa Clínica Integrada
Recruiting
Phase 1
Assessment of immediate and prolonged skin irritation and / or allergy.Healthy VolunteersM01.774.500RBR-72tgnyMedcin Instituto da Pele Ltda.
Not yet recruiting
Not Applicable
Assessment of skin irritability after using a health product responsible for reinforcing the skin's protection barrier, preventing microorganisms that cause skin diseasesAccidental InjuryNon-penetrating WoundsPenetrating WoundsDermatopathiesRBR-7jc7btrMedicin Instituto da Pele Ltda
Not yet recruiting
Not Applicable
Assessment of skin irritabilityRBR-5qyszr9Medicin Instituto da Pele Ltda