CTRI/2021/05/033863尚未招募不适用
A Pre-clinical and Clinical Study to evaluate the efficacy ofAshwagandhadi Avaleha as an Adjuvant in the management ofTuberculosis with Anti Tubercular Treatment.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- Principal
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Efficacy of Ashwagandhadi Avaleha to reduce/prevent toxicity when administered as add on therapy
研究概览
简要总结
I would like to publish my trial after completion of the trial as soon as possible. Patients will be selected from OPD/IPD of R.G.G.P.G. Ayurvedic College & Hospital, Paprola.
Two groups of 60 patients will be assessed to evaluate the efficacy of Ashwagandhadi Avaleha as an Adjuvant in management of Tuberculosis along with Anti Tubercular Treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 15.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Freshly diagnosed cases of tuberculosis(Pulmonary Tuberculosis and Tubercular pleural effusion)
- •Patients of either sex between the age of 15-70 years.
- •Patients willing and able to participate for 8 weeks duration.
排除标准
- •MDR and XDR cases of tuberculosis.
- •Patient with uncontrolled hypertension.
- •Suffering from any other chronic infections including HIV.
- •Patients Below the age of 15yrs and above the age of 70yrs.
- •Patients not willing for trial.
- •Individuals who have completed participation in any other clinical trial during the past three months.
- •Any other condition which the Principal investigator thinks may jeopardize the study.
结局指标
主要结局
Efficacy of Ashwagandhadi Avaleha to reduce/prevent toxicity when administered as add on therapy
时间窗: 8 weeks
along with Anti tubercular drugs in the management of Tuberculosis
时间窗: 8 weeks
次要结局
- Efficacy of the Ashwagandhadi Avaleha in improving general well being.(8 weeks)
研究者
研究点 (1)
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