跳至主要内容
临床试验/CTRI/2024/08/072348
CTRI/2024/08/072348尚未招募2/3 期

A Randomized Controlled Clinical study to evaluate the efficacy of Vachadi Choorna in Karshya

Dr Pawar Anuja Samindar1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年11月1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
To assess the weight gain depending upon subjective and objective parameters

研究概览

简要总结

The study is randomized, controlled, comparative clinical study  with the standard drug Masha Ashwagandhadi Choorna and Interventional drug Vachadi Choorna with the dosage of 6 gms for 5 to 7 years and 9 gms for 8 to 10 years , twice a day before food with anupan of Dugdha for Masha Ashwagandhadi group and Ghrita for Vachadi Choorna group. The study is conducting on subjects of Karshya belonging to age of 5 to 10 years who has given written and verbal concent by parents for underrgoing clinical study. Study will be conducting in Alvas Ayurveda medical college and Hospital moodubidri. Interventional period of this study is 90 days, assessment will be done before treatment,  30th, 60th, and 90 th 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
5.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • INCLUSION CRITERIA: a.
  • Subject irrespective of gender, religion, and socioeconomic status.
  • Age group – 5 to 10 years.
  • Grade 1(71-80%) and Grade 2(61-70%), IAP Classification of malnutrition (Based on weight for age of standard.).

排除标准

  • By assessing the clinical signs and symptoms, subjects with Systemic illness and Endocrine disorders, Subjects of known Congenital anomalies and Genetic defects will be excluded.

结局指标

主要结局

To assess the weight gain depending upon subjective and objective parameters

时间窗: 90 Days

次要结局

  • To improve the nutritional status.(90)

研究者

发起方
Dr Pawar Anuja Samindar
申办方类型
Other []
责任方
Principal Investigator
主要研究者

Dr Pawar Anuja Samindar

Alvas Ayurveda medical college and Hospital

研究点 (1)

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