“A Comparative study to evaluate the efficacy of Vamana Dhauti and Kushmanda(Benincasa hispida) Rasa in Amlapitta- A Randomized Clinical Trialâ€
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Vamana Dhauti and Kushmanda Rasa are expected to allievate Amlapitta
研究概览
简要总结
In this randomized Clinical Trial,we are going to compare the efficacy of Kushmanda Rasa and Vamana Dhauti in the patients of Amlapitta.With a total sample size of 60 patients,the study focuses on reduction in the symptoms of Amlapitta as the primary measure by dividing the total participants into two groups,with 30 in each of them.One group will be given Kushmanda Rasa and other will be given Vamana Dhauti.Assessment will be recorded on Day 1 (before treatment),Day 11,Day 21.The trial will be conducted in Ch. Brahm Prakash Ayurved Charak Sansthan, Khera Dabar,Delhi.
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 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Classical symptoms of Amlapitta.
- •2.Patients willing and able to carry out treatment for 21 days.
- •3.Patients will be registered with duly signed informed consent prior to the trial.
排除标准
- •1.Patients with diagnosed cases of gastric, peptic and duodenal ulcers.
- •2.Patients with any GIT, abdominal complications and chronic illness.
- •3.Patients with diagnosed cases of any systemic disorder.
- •4.Pregnant and lactating women.
- •5.Patients suffering from raised intracranial pressure, hernia, diabetes with eye problems, heart diseases.
结局指标
主要结局
Vamana Dhauti and Kushmanda Rasa are expected to allievate Amlapitta
时间窗: 1st Assessment on Day 1 | 2nd Assessment on Day 11 | 3rd Assessment on Day 21
次要结局
- Improvement in Subjective Parameters(1st Assessment on Day 1)
研究者
Dr AMRUTHA JAYAN
Ch. Brahm Prakash Ayurved Charak Sansthan