Randomized controlled clinical trial to compare the efficacy of oral administration of dashamool syrup with iron syrup in panduroga (anemia) in children
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Decrease in pandutwa, duration og play, aruchi, shwasa, hridyaspandan, shotha, constipation.
研究概览
简要总结
The study will be intervened by the treatment of Dashamoola Syrup and Iron Syrup to group A and group B respectively. The efficacy of the therapy will be assessed on the basis of subjective criteria for statistical analysis. Scoring will be designed according to the severity of symptoms. The subjective gradation of symptoms will be done as follows and the intensity of each symptom will be calculated before treatment, after treatment and after follow up. The effect of treatment result will be assessed in regards to clinical signs and symptoms on the basis of grading and scoring system. The signs and symptoms will be assessed by adopting the suitable scoring method.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- None
入排标准
- 年龄范围
- 2.00 Year(s) 至 12.00 Year(s)（—）
- 性别
- All
入选标准
- •Children presenting with classical signs and symptoms of Panduroga (Anemia).
- •Children with hemoglobin percentage between 8 to13 g/dl.
排除标准
- •Children with severe known case of anemia due to systemic disorders, Hemorrhagic diseases like Hemophilia, Vitamin k deficiency and Anemia due to other than nutritionaldeficiency.
- •Known case of hereditary Anemia.
- •Children with known case of concurrent serious hepatic dysfunction and renal dysfunction and uncontrolled Pulmonary Dysfunction.
- •H/O sensitive to any of the trial drugs.
- •Anemia with any associated severe complications.
结局指标
主要结局
Decrease in pandutwa, duration og play, aruchi, shwasa, hridyaspandan, shotha, constipation.
时间窗: 15 days
次要结局
- Decrease in pandutwa, duration og play, aruchi, shwasa, hridyaspandan, shotha, constipation.(30 days)
研究者
Adesh Charandaspant Raut
Tilak Ayurved Mahavidyalaya