跳至主要内容
临床试验/CTRI/2021/12/038769
CTRI/2021/12/038769尚未招募2/3 期

A comparative clinical trial to evaluate the efficacy of Eranda Sneha (Castor oil) at two different administration time as Pragbhakta and Nishi Kaala as Virechan Dravya in management of Malavarodha.

Sane Guruji Arogya kendra1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年12月24日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
40
试验地点
1
主要终点
The effect of Eranda Sneha as Virechan dravya in management of Malavarodha when given at Pragbhakta Kaala than Nishi Kaala in a dose of 5 ml for duration of 7 days.

研究概览

简要总结

This study is randomised comparative clinical trial to evaluate the efficacy of Eranda sneha (castor oil) as Virechan dravya in management of Malavarodha when given at Pragbhakta and Nishi Kaala. Primary outcome of study will be the effect of Eranda sneha as Virechan dravya in management of Malavarodha when administred in Pragbhakta Kaala than Nishi Kaala in dose of 5ml for duration of 7 days.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Not Applicable

入排标准

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

入选标准

  • Patients having symptoms of Malavarodha as per mentioned Rome II criteria and ODS Longo score for constipation at least since 1 week but not manifested with any other classical disease.

排除标准

  • IBS related patients
  • Patients diagnosed with piles
  • Iron supplements
  • Intestinal obstruction and acute abdomen.

结局指标

主要结局

The effect of Eranda Sneha as Virechan dravya in management of Malavarodha when given at Pragbhakta Kaala than Nishi Kaala in a dose of 5 ml for duration of 7 days.

时间窗: The drug will be given for 7 days. Patient will be called for follow up on 8th day as last dose of medicine will be on 7th day at night and on 15th day to check the after effect of drug

次要结局

  • Relief from symptoms of Malavarodha(The drug will be given for 7 days. Patient will be called for follow up on 8th day as last dose of medicine will be on 7th day at night and on 15th day to check the after effect of drug)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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