Efficiency And Safety Of Association Arbutin, Triamcinolone And Tretinoin In The Treatment Of Facial Melasma, Taking As Reference The Product Triluma ® (Hidroquinone, Fluoncinolone And Tretinoin).
试验速览
- 阶段
- 2 期
- 状态
- 暂停
- 入组人数
- 110
- 试验地点
- 1
- 主要终点
- evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone)in the treatment of epidermal melasma.
研究概览
简要总结
The objective of this study is evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone) in the treatment of epidermal melasma.
详细描述
The melasma is a common hipermelanosis, acquired, symmetrical, with irregular occurring in areas such as photo-exposed face, forehead and temples, can affect the eyelids and tion. The facial regions most affected are: zigomatic (82.4%), parotid (64.7%), front (64.7%), mandible (35.3%) and nasal (35.3%). The injuries of melasma is variable increase of epidermal melanin and inflammatory infiltrate of mild to moderate intensity. Treatment with compounds such as hydroquinone and derivatives, tretinoin, corticosteroids moderate or combination of them all have shown good results, diminishing the training, reducing the stability and promoting the destruction of melanocytes. The primary objective of this study is evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone) manufactured by Glenmark Laboratory, and as the comparator drug product Triluma ® (hydroquinone + fluocinolone + tretinoin), in the treatment of epidermal melasma through parameters of clinical course of the disease (improves) and its security.
Patients who are included in the study will be randomly and automatically receive one of the treatments (New association or Triluma ®), which should use for 12 weeks. The products should be applied in the regions affected once a day, during night.
The evaluation of clinical improvement, as well as security, will be held on periodic visits, as described below, which will be held the record and supply of medicines to patients.
In each visit, beyond the clinical examination of photographs and large, it filled the Area and Severity Scale (Melasma Area and Severity Index - MASI), which quantifies the melasma and will be the main tool of control of clinical improvement.
At the end of the study, data will be compared, showing no inferiority or inferiority of clinical drug testing in relation to the comparator.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women adults aged more than 18 years;
- •Patients suffering from melasma Epidermal the face of mild and moderate;
- •Patients who have not done any treatment for melasma in the 3 months preceding the study;
- •Patients with good mental and physical health;
- •Patients who agree with the purposes of the study and sign the TCLE.
排除标准
- •Patients with skin diseases other than melasma, which interfere in clinical evaluation as hemangiomas and queloides;
- •Patients with melasma skin or mixed;
- •Patients with sensitivity to agents hipopigmentantes;
- •Patients with sensitivity to fotoprotetores;
- •Patients who are pregnant or breastfeeding;
- •Patients who, at the discretion doctor, are not able to participate in the study;
- •Patients who have carried out any treatment for melasma in the 3 months preceding the study
- •Patients who do not agree with the terms described in the Statement of Informed Consent
研究组 & 干预措施
1
arbutin, tretinoin, triamcinolone
干预措施: arbutin, tretinoin, triamcinolone (Drug)
2
Triluma
干预措施: Triluma (Drug)
结局指标
主要结局
evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone)in the treatment of epidermal melasma.
时间窗: arbutin triamcinolone tretinoin
次要结局
未报告次要终点
研究者
Azidus Brasil
Principal Investigator Dr. Alexandre Frederico
Azidus Brasil