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临床试验/CTRI/2023/11/059678
CTRI/2023/11/059678已完成2 期

A comparative clinical study to evaluate the efficacy of Agnikarma and Siravyadha in Yakriddalyudara vis-a-vis Fatty liver disease

Dr Megha R1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年11月13日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Change in ultra sonography reading and SGOT, SGPT level, Weight, reduce in Klama, Adhmana, agnimandya and hritkanta daha after 15 days of completion of 4th sitting of the procedure

研究概览

简要总结

A comparative clinical study to evaluate the efficacy of Agnikarma and Siravyadha in yakkriddaludara vis-a-vis fatty liver disease.

Subjects fulfilling subjective and objective criterias will be choosen for the study, one group consisting of 20 subjects will be treated with Agnikarma at dakshina manibandha (right anatomical snuff box) another group of 20 subjects will be treated with siravyadha at dakshina kurpara sandhi(right cubital region) for 4 sitting each with a gap of 7 days and follow up will be done after 45 days of first sitting.

After completion of the treatment, Group B that is the subjects treated with Siravyadha showed better result.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

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

入选标准

  • Sonologically diagnosed case of grade 1 and grade 2 fatty liver disease.

排除标准

  • Uncontrolled DM and HTN, suffering with other systemic disorders.

结局指标

主要结局

Change in ultra sonography reading and SGOT, SGPT level, Weight, reduce in Klama, Adhmana, agnimandya and hritkanta daha after 15 days of completion of 4th sitting of the procedure

时间窗: At baseline, 1st week, 2nd week, 3rd week, 4th week and 6th week

次要结局

  • Objective criterias like USG, SGOT SGOT, Weight(At base line & After 15 days of completion of treatment i.e., on 6 weeks)

研究者

发起方
Dr Megha R
申办方类型
Other [self]

研究点 (1)

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