CTRI/2021/08/035349尚未招募3 期
PHARMACEUTICAL STANDARDISATION OF VISHATINDUKA TAILAM AND ITS EFFECT ONGRIDHRASI
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Assessment will be done based on Oswestry low
研究概览
简要总结
To prepare and carry out the pharmaceutical study of Vishatinduka tailam as per Reference ofBhasavarajiyam in vataroga nidhana lakshana chikitsadyaya.To analyse and standardize theVishatinduka tailam prepared. To carry out the clinical trial on Gridhirasi by using Vishatindukatailam.And to analyse whether vishatindukatailam is effective in pain relief.
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)(—)
入选标准
- •Patient irrespective of Gender and Occupation will be selected.
- •Patient age between 18-60 years.
- •Patient willing for study and follow up.
排除标准
- •Patient suffering from Structural deformity like lordosis, kyphosis and scoliosis (After doing physical examination of back including inspection, palpation, gait).
- •Patient under pediatric age group and those who are above 60 years.
- •Patient suffering from any systemic disease like diabetic mellitus, hypertension, thyroid dysfunction or the patient under any concomitant medications.
- •Any neoplasms like osteoma and myeloma.
结局指标
主要结局
Assessment will be done based on Oswestry low
时间窗: 1 WEEK
Schobers Test
时间窗: 1 WEEK
back pain disability questionnaire.
时间窗: 1 WEEK
SLR Test – Active and Passive
时间窗: 1 WEEK
次要结局
- analyse effect of vishatinduka tailam in sciatica(2 WEEKS)
研究者
研究点 (1)
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