A Comparative Clinical Study to evaluate the efficacy of Simhnad Guggulu And Panchamrita Lauha Guggulu along with Amalakadi Choornam in the management of Manyastambha
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 140
- 试验地点
- 1
- 主要终点
- Reduction in Ruk(Pain), Stambha(Stiffness) of Manyapradesha.
研究概览
简要总结
The present study is an interventional, open label, parallel group trial which aims to evaluate and compare the efficacy of Simhanad Guggulu and Panchamrita lauha guggulu along with Amalakadi choornam in the management of manyastambha. One hundred and forty patient aged 20 - 60 years with classical features of mayastambha will be randomly categoriesd in two groups i.e 70 patients in each groups. In both groups for amapachana Amalakadi Choornam will be given for 5 days which is followed by simhanad Guggulu 500mg BD in Group A for 60 days. while in Group B after Amapachan Panchamrita lauha Guggulu 500mg BD for 60 days will be given.for both groups Ashtavargam Kashyam 30 ml is used as anupana for guggulu kalpas.After medication patient will observed for 30 days in both groups. So overall study duration becomes 95 days and followup will be done after 15 days .
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Open Label
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Subjects between the age group of 20 to 60 years.
- •The subjects with classical signs and symptoms of Manyasthamba .
- •Subjects of all genders, irrespective of religion and caste.
排除标准
- •Patients below 20 and above 60 years of age.
- •Pregnant and lactating mother.
- •Subjects with other systemic disorders such as accelerated hypertension, uncontrolled diabetes, gastritis, acid peptic disorder, hypothyroidism that interfere in the line of treatment.
- •Subjects with congenital deformity, traumatic injuries, cervical stenosis & myelopathy, ankylosing spondylitis, infections of bones, and gross bony deformity.
- •Patient suffering from autoimmune joint disorders.
结局指标
主要结局
Reduction in Ruk(Pain), Stambha(Stiffness) of Manyapradesha.
时间窗: 95days
次要结局
- Improvement in pain Vas Score, Neck disability index score and Neck range of movement(95 days)