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临床试验/CTRI/2026/04/108142
CTRI/2026/04/108142尚未招募2/3 期

A RANDOMISED CONTROLLED CLINICAL TRIAL TO COMPARE THE EFFICACY OF ORAL ADMINISTRATION OF BHARANGYADI AVLEHA WITH KARPURADI AVLEHA IN VATAJ KASA IN CHILDREN WITH AGE GROUP 5 TO 12 YEARS.

TILAK AYURVED MAHAVIDYALAYA1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年4月22日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
60
试验地点
1

研究概览

简要总结

The study will be intervened by the treatment of Bharangyadi avaleha  and Karpuradi avaleha to group A and group B respectively. The efficacy of the therapy will be assessed on the basis of subjective and objective criteria for statistical analysis. Scoring will be designed according to the severity of symptoms. The subjective and objective gradation of symptoms will be done as follows and the intensity of each symptom will be calculated before treatment, after treatment and after follow up. The effect of treatment result will be assessed in regards to clinical signs and symptoms on the basis of grading and scoring system. The signs and symptoms will be assessed by adopting the suitable scoring method.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
5.00 Year(s) 至 12.00 Year(s)(—)
性别
All

入选标准

  • Children having symptoms of Vataj kasa.
  • Children of age group 5 year to 12 years.
  • Acute cough of maximum duration upto 7 days.

排除标准

  • Chronic dry cough, productive cough, any other disease of respiratory tract like LRTI, COPD, Asthama, Emphysema and febrile conditions, etc.
  • Age less than 5 year and greater than 12 years.
  • Children having respiratory distress.

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Shubhangi Rajesh Nalawade

Tilak Ayurved Mahavidyalaya

研究点 (1)

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