Comparative study on clinical evaluation of Mayiliragaadhi chooranam (internal ) and Kandangkathiri ennai (external)versus kandangkathiri Ennai (external)only-a siddha drug for Venpadai(vitiligo)- as Pilot study.
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Reduction of the hypopigmented lesions in the affected area
研究概览
简要总结
It is an Open clinical trial, to evaluate the therapeutic efficacy of Mayiliragadhi chooranam internal medicine and kandangathiri ennai external medicine from the siddha texts gunapadam thaadhu and mooligai vaguppu. Theingridients are thippili ,seeragam,mayiliragu 1gm b.i.d orally with honey for 48 days and kandankathiri pazha chaaru with olive oil external medicine. The treatment will be given for 48 days. The Laboratory investigationsand Clinical assessments will be recorded periodically before and aftertreatment period. All the trial related data will be recordered in Case ReportForm (CRF) for each patient separately. At the end of trial all the data will beanalysed statistically and the research reports will be Published
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 5.00 Year(s) 至 12.00 Year(s)（—）
- 性别
- All
入选标准
- •Age: Between 5 to 12 years Sex: Both male and female children Hypo pigmented patches with hyper pigmented border without any structural changes in any part of the body Willing to co operate for taking photographs whenever required with hisher consent.
排除标准
- •1.Albinism 2.Thyroid disorder 3.Leprosy 4.HIV 5.Fungal infestation 6.Burns Patient with lesion in the lips ,sole , palm and genitalia.
结局指标
主要结局
Reduction of the hypopigmented lesions in the affected area
时间窗: 45 days after medications
次要结局
- Reduction in the recurrence rate of the lesions.(after 48 days)