CTRI/2021/09/036825已完成2/3 期
A Comparative Clinical Study of Gunjaphaladi Lepa and Avalgujbeejadi Lepa in the management of Kilaasa (Vitiligo)
Government Ayuvedic College Patna1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年1月10日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- The assessment will be based on the color, size,VETF, VIDA score, margins of the lesion and % of area involvement of the white patches.
研究概览
简要总结
In this study, 60 clinically diagnosed and confirmed patients of kilaasa (vitiligo) will be divided into 2 groups of 30 patients each.
Group I will be given Gunjaphaldi lepa and Group II will be given Avalgujbeejadi lepa.
The data will be collected and assessed by different scales of measurement. 6 evaluation will be done by follow up after every 15 days
The patients will be evaluated on the basis of subjective and objective parameter to assess the efficacy of the intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 12.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •as per classical sign and symptoms described in ayurvedic texts and modern literature.
- •Prediagnosed patient of Kilaasa(vitiligo).
排除标准
- •Patients below 12 yrs.
- •and above 60 yrs.
- •Chronicity of kilaasa more than 5 yrs.
- •Patients associated with diabetes, AIDS, Hep-B, leukemia -Pregnant women/lactating women -white anesthetic spots which are character of leprosy.
结局指标
主要结局
The assessment will be based on the color, size,VETF, VIDA score, margins of the lesion and % of area involvement of the white patches.
时间窗: Patients will be followed up after 15 days up to 3 months of trial.
次要结局
- Improvemeent in the quality of kilaasa(vitiligo)(Evaluation will be done after 90 days.)
研究者
研究点 (1)
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