CTRI/2025/08/092964尚未招募3 期
Randomised Controlled Clinical Trial to Determine Efficacy of Aragvadhamrutadi Kashaya in Management of Amlapitta w.s.r.to Non-Ulcer Dyspepsia
SST Ayurved Mahavidyalaya Sangamner1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年8月24日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Randomized controlled clinical trial to determine efficacy of
研究概览
简要总结
it is randomized controlled clinical trial to determine efficacy of
Aragvadhamrutadi Kashaya in management of Amlapitta w.s.r. to Non-Ulcer Dyspepsia with age group 18-50 years both in male and females included 40 patients in each trial and control group.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •1 All the patients with sign and symptoms of Amlapitta like Avipak, Klama(Tiredness), Utklesh(Nausea), Tikta-amla Udgar(Bitter-sour belching), Gaurava(Abdominal heaviness), Hrud-Kanth Daha, Aruchi.
- •2 Patients who are ready to sign inform consent form.
- •3 patients with age group 18 to 50 years irrespective of sex.
排除标准
- •1 Known case of bleeding disorders, CA stomach patients.
- •2 Known case of severe systemic disorder and endocrine disorder like DM, Thyroid disorder patients.
- •3 Lactating and pregnant women.
- •Known case of TB, HIV, Hiatus-hernia, achalasia cardia.
- •Known case of Helicobacter Pylori infection.
结局指标
主要结局
Randomized controlled clinical trial to determine efficacy of
时间窗: 18 Months
Aragvadhamrutadi Kashaya in management of Amlapitta w.s.r. to Non-
时间窗: 18 Months
Ulcer Dyspepsia.
时间窗: 18 Months
次要结局
- relief of amlapitta symptoms(4 weeks)
研究者
Savita Potalaji Kamle
SSTs Ayurved Mahavidyalaya,Sangamner
研究点 (1)
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