跳至主要内容
临床试验/CTRI/2025/01/079110
CTRI/2025/01/079110招募中2/3 期

An open label double arm randomized comparative clinical study on the efficacy of madanphala triphaladi kashayam and gomutra haritaki vati in sthaulya

DR Ajay Shinde1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年2月2日最近更新:

试验速览

阶段
2/3 期
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
To evaluate the efficacy of Madanphala Triphaladi Kashayam & Gomutra Haritaki Vati in Sthaulya

研究概览

简要总结

This is an Open Label Double Arm Randomized Comparative Clinical Study on the Efficacy of Madanphala Triphaladi Kashayam and Gomutra Haritaki Vati in Sthaulya which is being conducted in Dhanvantari Ayurveda College and Hospital, Siddapur Karnataka as part of PG thesis. The subjects will be divided into two groups, each comprising of 20 patients and will be intervened with both trial as well as standard drug for a duration of 30 days to assess its efficacy in Sthaulya Roga and the parameters will be assessed every 7 days once during the duration of intervention

研究设计

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

入排标准

年龄范围
16.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients having cardinal signs and symptoms of sthaulya.
  • B.M.I. 25 to 39.9 kg/m
  • Willing to give written informed consent.

排除标准

  • 1.Age below 16years and above 60years 2.Diagnosed cases of Diabetes, Cardio pulmonary diseases, Thyroid disorders, Parkinsonism 3.Pregnant and Lactating women 4.B.M.I below 25kg/m2 and above 40kg/m2.

结局指标

主要结局

To evaluate the efficacy of Madanphala Triphaladi Kashayam & Gomutra Haritaki Vati in Sthaulya

时间窗: 0 15 31 days

次要结局

  • To compare the efficacy of both Madanphala Triphaladi Kashayam & Gomutra Haritaki Vati in Sthaulya(0, 14 & 31st days)

研究者

发起方
DR Ajay Shinde
申办方类型
Other [Self ]

研究点 (1)

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