CTRI/2024/09/074512尚未招募2 期
Clinical validation of Unani pharmacopoeial formulation Majoon Mussaffi Azam in Busoor(Skin eruptions)
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- The lesion will be evaluated according to its number, size, and associated symptoms. Grading on the basis of the number of lesions will be recorded
研究概览
简要总结
it is a single arm open labelled study in which patients visiting OPD with the complaints of Busoor willing to undergo trial and fulfilling the inclusion criteria will be recruited. after screening the drug will be given orally for30 days.the efficacy and safety will be checked accordindly
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 12.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- Female
入选标准
- •Frequently occurrence of Busoor, with or without association of following features.
- •1.Humra (Erythema) 2 .Waja (Pain)
- •Hikka (Itching.
排除标准
- •1 .Patients of Busoor associated with fever.
- •Patients with other inflammatory and suppurated conditions of skin e.g. Abscess, Carbuncle, and Cellulitis.
- •3.Patients with features of Cellulitis 4.Patients with diabetes mellitus 5.Patients with disease required long term treatment e.g. Metabolic Disorders, specific infectious disease and cancer etc.
- •6.Pregnancy and lactation.
结局指标
主要结局
The lesion will be evaluated according to its number, size, and associated symptoms. Grading on the basis of the number of lesions will be recorded
时间窗: Baseline,Day 7,Day 14,Day 28
次要结局
未报告次要终点
研究者
Dr Huma
Regional research institute of unani medicine
研究点 (1)
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