跳至主要内容
临床试验/CTRI/2019/02/017470
CTRI/2019/02/017470招募中不适用

Randomized comparative clinical study of vajigandhadi taila matra basti and pana in the management of gridhrasi w.s.r lumbosacral radiculopathy

Rishikul campus1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年8月2日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group.

研究概览

简要总结

Trial is going on..

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
25.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Daignosed cases of gridhrasi(lumbosacral radiculopathy) Patient daiagnosed of lumbago based upon investigation History of lumbosal sprain/strain/ lumbago for more than six months.

排除标准

  • Uncontrolled diabetes mellitus Uncontrolled T.B.of spine & hip joint Uncontrolled hypertention Malignancy of spine or other or organs Fracture related to spine Cardiac disease(IHD, CAD, MI etc) Anaemic(Hb% less than 7.00 mg/dl) Pregnancy Age group less than 20 years and greater than 60 years Refferred low backache from pelvis, abdomen or thoracic disease.

结局指标

主要结局

Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group.

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

Moderately improved-51-75%

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

Improved - 26-50%

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

Complete remission-100%

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

Unchanged - 0-25%

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

Markedly improved-76-99%

时间窗: Only objective parameters will be employed for the assessment of the impact of treatment procedures in the respective group. | Complete remission-100% | Markedly improved-76-99% | Moderately improved-51-75% | Improved - 26-50% | Unchanged - 0-25%

次要结局

  • Excerbation in sign & symptoms(42 days)

研究者

发起方
Rishikul campus
申办方类型
Research institution and hospital

研究点 (1)

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