NCT05508243已完成不适用
Dermatologist-supervised Assessment of Primary and Accumulated Irritation Potential and Skin Sensitization Potential for the NASAL SPRAY Product
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 65
- 试验地点
- 2
- 主要终点
- Absence
研究概览
简要总结
Evaluate the potential of Primary Dermal Irritability, Accumulated Dermal Irritability and Dermal Sensitization, of health products through the application of Patch Test, proving the safety of the product for topical use. The study will be conducted with a Brazilian sample in which 65 research participants will be included. Depending on the results, the present study may support the claim: dermatologically tested.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy research participant
- •Age range between 18 and 70 years.
- •Gender: female and male.
- •Phototype (Fitzpatrick): I to IV.
- •Agree to adhere to the requirements of the study in the fight against the COVID-19 pandemic, through preventive measures: use a mask according to WHO guidelines; use the mask while traveling to the research center and during the study procedures; maintain social distancing; wash hands frequently with soap and/or alcohol gel and go to the research center only at scheduled times to avoid agglomerations.
- •Agree not to wet the site during the entire test period;
- •Understand the test procedures and agree to their adherence to the study requirements;
- •Absence of inflammatory dermatoses or tattoo at the application site;
- •Signing of the Free and Informed Consent Term (FICT).
排除标准
- •Pregnancy, lactation;
- •Participants with hyperthermia (body temperature greater than or equal to 37.5ºC);
- •Participants who have been diagnosed with COVID-19 by RT-PCR exam or by the presence of IgM antibodies in the serology exam, in the last 4 weeks or who are presenting the following symptoms: dry or productive cough, sneezing, runny nose, body pain , headache, anosmia (loss of smell), ageusia (loss of taste) and/or any other symptom that may be related to covid-19 at the discretion of the investigator;
- •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;
- •Participants with heart disease (eg, but not limited to: atrial fibrillation, obstructive coronary artery disease);
- •Participants with renal and/or neurological diseases;
- •Participants with severe or decompensated lung and/or respiratory diseases;
- •Use of corticosteroids, antihistamines and/or anti-inflammatory drugs;
- •Presence of localized or generalized skin diseases;
- •Presence of active inflammatory dermatoses in the test region;
- •Frequent exposure to the sun or tanning beds;
- •Have participated in an allergenicity study within a period of less than four weeks from the beginning of the study;
- •Research participants with a history of allergy to the material used in the study;
- •Atopy history;
- •History of pathologies aggravated or triggered by ultraviolet radiation;
- •Immunodeficiency carriers;
- •Forecast of intense sun exposure or tanning session during the study period;
- •Forecast to take a bath in the sea, swimming pool or sauna during the study;
- •Research participants who practice water sports;
- •Research participants with dermographism;
- •Use of the following topical or systemic medications: immunosuppressants, antihistamines, non-steroidal anti-inflammatory drugs, and corticosteroids up to 2 weeks before selection;
- •Treatment with acidic vitamin A and/or its derivatives orally or topically up to 1 month before the start of the study;
- •Aesthetic and/or dermatological body treatment up to 03 weeks before selection;
- •Vaccination forecast 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;
- •History of non-adherence or unwillingness to adhere to the study protocol;
- •Professionals directly involved in carrying out this protocol and their families.
- •Be participating in some other study at the moment.
- •Any condition that, in the opinion of the researcher, could compromise the study.
结局指标
主要结局
Absence
时间窗: 6 weeks
Absence occurence of phototoxicity and photoallergy
次要结局
未报告次要终点
研究者
研究点 (2)
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