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临床试验/CTRI/2024/05/067471
CTRI/2024/05/067471尚未招募2 期

Pharmaceutico Clinical Study Of Marichadi Taila And Vidangadi Guggulu On Pama Kustha W.S.R To Scabies

Dr Jayanta Bag1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年5月25日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To evaluate the effect of Marichadi tails & vidangadi Guggul on Pama Roga w.s.r to scabies in clinical trail.

研究概览

简要总结

All the patients will be evaluated on the basis of their age, sex, religion, climatic condition,socio-economic status, education status, occupation, nature of work, economical status, marital status, Prakriti, Dosha, Agni, kostha, and subjective and objective parameters of an open label interventional prospective trail to study the pharmaceutico clinical study of Marichadi tails and vidangadi guggul on Pama kustha w.s.r to scabies in 2 groups each containing 30 patients. This study will be conducted in Government Ayurvedic College and Hospital, Patna, Bihar in the department of Rasa Shastra evam Bhaishajya Kalpana. After 07 days of intervention three  follow up will be done every 07 days for total duration of study i.e of 30 days.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
8.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patient willing for trial.
  • Selected sign and symptoms based on both Ayurvedic & modern context.
  • Age group between 08-70 year.

排除标准

  • Age above 08 year and below 70 years. Patients having any systemic illness like.
  • T: B, Hepatitis -B, AIDS etc. Pregnant women and lactating women.

结局指标

主要结局

To evaluate the effect of Marichadi tails & vidangadi Guggul on Pama Roga w.s.r to scabies in clinical trail.

时间窗: 30 days

次要结局

  • To see the preparation of safe, effective, and quality drug and standardization.(30 days)

研究者

发起方
Dr Jayanta Bag
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Jayanta Bag

Government Ayurvedic College And Hospital

研究点 (1)

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