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临床试验/CTRI/2024/12/077799
CTRI/2024/12/077799尚未招募2/3 期

A RANDOMIZED CONTROLLED CLINICAL STUDY TO EVALUATE THE EFFICACY OF KARAVIRADYA TAILA IN MANAGEMENT OF PAMA KUSHTA IN CHILDREN

DR ASHWITH A1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年12月13日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
40 sample size divided into 2 groups of 20 each group A and group B

研究概览

简要总结

The study is randomized, parallel group , activity controlled comparative clinical study with Durvadya Taila as standard drug and Karaviradya Taila as interventional drug with the dosage as quantity sufficient as external application for 10 days morning and evening for an hour followed by hotwater wash. This study will be conducted on subjects belonging to the age group 6-16 years who has given written and verbal consent by parents for undergoing clinical study. The study will be conducted in Alvas Ayurveda Medical College and Hospital, Moodubidire. Interventional period of study is 15 days and assessment will be done before treatment, 5th day, 10th day and follow up on 15th day.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
6.00 Year(s) 至 16.00 Year(s)(—)
性别
All

入选标准

  • Subject to fulfil the diagnostic criteria.
  • irrespective of gender, religion and socioeconomic status.
  • Age between the age group 6-16 years.

排除标准

  • Kustha other than Pama.
  • Subjects with any other systemic disorder.

结局指标

主要结局

40 sample size divided into 2 groups of 20 each group A and group B

时间窗: 2weeks(15 days)

次要结局

  • to reduce the outcome of(Shyava Aruna Varna pidika( black head papules , vesicles),)

研究者

发起方
DR ASHWITH A
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

DR ASHWITH A

Alvas Ayurveda Medical College and Hospital, Moodubidre ,Dakshina Kannada

研究点 (1)

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