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临床试验/CTRI/2017/05/008719
CTRI/2017/05/008719招募中不适用

A CLINICAL STUDY OF GUDUCHYADICHURNA AND ELADI CHURNA IN THE MANAGEMENT OF AMLAPITTA

GOVT AKHANDANAND AYURVED COLLEGE1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年5月23日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30
试验地点
1
主要终点
Result will be assessed on the basis of relief in the Signs and symptoms of Amlapitta

研究概览

简要总结

This study is a randomised, participants blinded, parallel group, active controlled trial to evaluate the efficacy of Guduchyadi Churna in aDose of  10gm/day two divided dose with water Duration: 4 weeks in 15 patients with GROUP A and also  to evaluate the efficacy of  Eladi Churna in aDose of  10gm/day two divided dose with water Duration: 4 weeks in 15 patients of GROUP B in Amlapitta.

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
16.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients with classical signs & symptoms of Amlapitta.Avipaka (Indigestion), Klama(Lassitude), Utklesha (Nausea), Tiktodgara(Bitter eruction), Amlodgara(sour eruction),Gaurav(heaviness of body),Hrit Daha(Heart buru), Kantha Daha (Burning in throat), Aruchi (Anorexia).

排除标准

  • Patients suffering from Hematemesis, Acute diarrhoea, Intestinal T.B, Gastric and Peptic ulcer, uncontrolled D.M. and HTN, Arsha, Carcinoma, cardiac disorders etc.
  • serious condition of the patient.

结局指标

主要结局

Result will be assessed on the basis of relief in the Signs and symptoms of Amlapitta

时间窗: 4 WEEKS

次要结局

  • Result will be assessed on the basis of relief in the Signs and symptoms of Amlapitta(4 weeks)

研究者

发起方
GOVT AKHANDANAND AYURVED COLLEGE
申办方类型
Government medical college

研究点 (1)

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