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临床试验/CTRI/2019/07/019965
CTRI/2019/07/019965已完成2 期

Clinical evaluation of the effect of KARAPPAN KUDINEER CHOORANAM(internal) and KODIVELI ENNAI(external) in the management of PORI KARAPPAN

I BIBINA1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年1月7日最近更新:
适应症

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
scaling, ertheyma, papules, vesiculation, oozing

研究概览

简要总结

The present study was performed as a single arm clinical trial to access the efficacy of karappÄṉ kuá¹­inÄ«r cÅ«raṇam(internal) and  koá¹­ivÄ“li eṇṇey(external) in the management of pori karappÄṉ. In this trial 40 patients were recruited and the trial drug were administered orally 15-30 ml twice a day after food and external application of oil for the period of 21 days. The primary outcome was accessed by changes in symptoms likeitching,erythema, papules, vesiculation, oozing and secondary outcome was accessed by the laboratory parameters like reduced ESR and absolute eosinophil count.

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

  • •severe itching erythema vesicles oozing lichenification.

排除标准

  • •children above 12 years urticarial rashes due to drug intake FDE urticarial associated with other severe form of dermatological disorder.

结局指标

主要结局

scaling, ertheyma, papules, vesiculation, oozing

时间窗: 15 days

次要结局

  • ESR(Total eosinophil count)

研究者

发起方
I BIBINA
申办方类型
Other [self]

研究点 (1)

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