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临床试验/CTRI/2025/01/079545
CTRI/2025/01/079545尚未招募不适用

A randomized controlled clinical trial to evaluate the effect of Erandamoola Kshara Basti in the management of Vata-Kaphaja Gridhrasi w.s.r. to Sciatica

未提供1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
试验地点
1
主要终点
Pain

研究概览

简要总结

A randomised clinical study to evaluate the effect of Erandamoola Kshara Basti in the management of Vata-Kaphaja Gridhrasi w.s.r. to Sciatica. In this study, total 30 patients will be taken in two groups. In Group-A, Erandamoola Kshara Basti is given to 15 patients by making patient  to lie down in a left lateral position with right lower limb flexed at the knee joint with extended left lower limb. The left hand is folded and used as a pillow under the head and Drug will be administered. In Group- B, Vaitarana Basti is given to 15 patients by making patient  to lie down in a left lateral position with right lower limb flexed at the knee joint with extended left lower limb. The left hand is folded and used as a pillow under the head and Drug will be administered. The study will be conducted at Sri Dharamasthala Manjunatheshwara College of ayurveda, hospital and research centre, Kuthpady Udupi. The primary outcome measures will be assessed by subjective and objective parameters. The secondary outcome measures will be assessed based on quality of life scale. Hence this study is an effort to prove the the efficacy of Erandamoola Kshara Basti in the management of Vata-Kaphaja Gridhrasi w.s.r. to Sciatica.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Subjects fulfilling the diagnostic criteria subject fit for basti karma.

排除标准

  • Subjects with any systemic diseases which may interfere with the course of treatment will be excluded.

结局指标

主要结局

Pain

时间窗: 0th day, 8th day and 16th day

Pricking pain

时间窗: 0th day, 8th day and 16th day

Stiffness

时间窗: 0th day, 8th day and 16th day

Drowsiness

时间窗: 0th day, 8th day and 16th day

Loss of appetite

时间窗: 0th day, 8th day and 16th day

Heaviness

时间窗: 0th day, 8th day and 16th day

Objective parameters

时间窗: 0th day, 8th day and 16th day

Straight Leg Raising test

时间窗: 0th day, 8th day and 16th day

Lassegue Test

时间窗: 0th day, 8th day and 16th day

Bragard Test

时间窗: 0th day, 8th day and 16th day

Primary outcome will be assessed based on the following parameters

时间窗: 0th day, 8th day and 16th day

subjective parameters

时间窗: 0th day, 8th day and 16th day

次要结局

  • Quality of life(0th & 24th day)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Bhuvaneshwari V Rathod

Sri Dharamasthala Manjunatheshwara College of Ayurveda Hospital and Research Centre Kuthpady Udupi

研究点 (1)

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