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
研究点 (1)
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