CTRI/2022/08/044766已完成3 期
A Prospective, Open-Label, Single Arm Study To Evaluate The Safety And Efficacy Of Bakutrol Face Cream For Its Anti-Acne Effect In Otherwise Healthy Male Or Female Volunteers
Viridis Bioharma Pvt Ltd0 个研究点目标入组 50 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Male and female patients aged 18 to 35 years
- •2.Diagnosis of moderate facial acne vulgaris
- •3.Phototype I II III or IV according to Fitzpatrick classification
- •4.Facial inflammatory lesion count grater than 20 and
- •5.Non inflammatory lesions count of at least 20-100
- •6.Investigators Global Assessment score 3
排除标准
- •1.Patients with 2 nodulocystic lesions, prior topical acne treatment or systemic anti-inflammatory agents in past 14 days.
- •2.Patients on systemic corticosteroids, antibacterial, immunosuppressant drugs or abradant facial procedures in the past 30 days
- •3.Patients with other concurrent facial skin disease and patients who are photosensitive or who are likely to engage in activities that involve excessive or prolonged exposure to sunlight.
- •4.Patients with drug induced acne
- •5.Patients with menopausal disorders
- •6.Has a history of significant reactions to topical acne treatments, or a known allergy or hypersensitivity to any listed ingredients
- •7.Use of oral retinoid within 6 months of Baseline visit.
研究者
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