跳至主要内容
临床试验/CTRI/2021/01/030317
CTRI/2021/01/030317已完成2 期

Clinical Evaluation of the Effect on Oral Administration of VATHA KARAPPAN CHOORANAM along with external Administration of SIVAPPU ENNAI in the Management of VATHA KARAPPAN

Dr v Sindhu1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年1月14日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Decrease the frequency of severe itching,erythema,vesicles ,oozing and other clinical symptoms

研究概览

简要总结

It is a Single Arm Clinical Trial to determine the safety and efficacy of VATHA KARAPPAN CHOORANAM (Oral administration) along with SIVAPPU ENNAI(External administration) in patients with VATHA KARAPPAN.The outcome will measured by day 1,week 1 week 2, week 3 intervals.During this period if any adverse effect and serious adverse effect will be noticed and referred to pharmacovigilence department in Government siddha medical college and hospital, Palayamkottai and for the management will also be given in department of Kuzhanthai maruthuvam OPD and IPD. After the completion of trial all the study related data will be analysed statistically.

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
2.00 Year(s) 至 12.00 Year(s)(—)
性别
All

入选标准

  • Subject with any of the following symptoms will be included in the study 1.Severe Itching 2.Erythema 3.Vesicles 4.Oozing 5.Lichenification.

排除标准

  • 1.Children above 12 years 2.Fungal Infection 3.Bullous formation in skin 4.Congenital Dermatological disorders.

结局指标

主要结局

Decrease the frequency of severe itching,erythema,vesicles ,oozing and other clinical symptoms

时间窗: 21 days

次要结局

未报告次要终点

研究者

发起方
Dr v Sindhu
申办方类型
Other [self]

研究点 (1)

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