CTRI/2018/02/012256已完成1 期
An Open Labelled, Single Arm Study To Evaluate The Efficacy Of Murvadya Choorna Vati In Pandu Vyadhi W.S.R. To Iron Deficiency Anaemia
Self1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年1月3日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Study the effect of Murvadya Choorna Vati on clinical symptoms and hematological parameters of Pandu Vyadhi.
研究概览
简要总结
“An open labelled, single arm study to evaluate the efficacy of murvadya choorna vati in Pandu Vyadhi W.S.R. to iron deficiency anaemiaâ€. The prevalence of Anaemia in 2016 is estimated at 9% in high developed country and 43% in developing country. The aim of the trial is to study the efficacy of Murvadya Choorna Vati in Pandu Vyadhi with special reference to Iron Deficiency Anaemia. The objectives are to evaluate the effect of Murvadya Choorna Vati in Pandu Vyadhi on the basis of change in Haemogram i.e. Hb%, RBC count, MCV, MCH, MCHC, HCT, RDW, Sr. Iron level and TIBC and clinical symptoms also.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Pandu Vyadhi will be diagnosed according to subjective & objective parameters.
- •Age : 18-60 Yrs.
- •Irrespective of gender, religion, socio-economic status, marital status
- •Hb % more than 8 gm% & less than normal i.e. Male -<13g / dl, Female – < 12g / dl.
排除标准
- •1.Endocrine disorders like hypothyroidism, Cushing syndrome, etc.
- •2.Pregnant and lactating lady.
- •3.Patient having tuberculosis, known case of HIV, leprosy, any type of Cancer.
- •4.Patients showing signs and symptoms of internal bleeding, hemorrhoids, menorrhagia or any other bleeding disorder.
- •(Worms, scurvy, puerperal etc.).
结局指标
主要结局
Study the effect of Murvadya Choorna Vati on clinical symptoms and hematological parameters of Pandu Vyadhi.
时间窗: 45 Days
次要结局
- To evaluate the effect of Murvadya Choorna Vati in Pandu Vyadhi on the basis of change in Haemogram i.e. Hb%, RBC count, MCV, MCH, MCHC, HCT, RDW, Sr. Iron level and TIBC and clinical symptoms also.(45 Days)
研究者
研究点 (1)
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