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临床试验/CTRI/2024/10/075221
CTRI/2024/10/075221尚未招募不适用

A randomized controlled clinical trial to evaluate the effect of vedanasthapana mahakashaya parisheka on pain parameter in amavata w.s.r. to rheumatoid arthritis

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: 2024年11月1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
Primary outcome will be assessed based on the following parameters

研究概览

简要总结

This is a randomized, open labelled, parallel group study comparing the efficacy of Controlled group - A , Twak Patra Parisheka which will be given to whole body without abhyanga once in a day for 7 days and the Trial group - B, Vedanasthapana Mahakashaya Parisheka which will be given to whole body without abhyanga once in a day for 7 days for 15 patients to each group and selection will be based on permuted block randomization method. The study will be conducted in 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 the quality of life scale. Hence this study is an effort to prove the efficacy of Vedanasthapana Mahakashaya Parisheka on pain parameter of Amavata w. s.r.  to Rheumatoid Arthritis.

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

  • Freshly diagnosed cases of rheumatoid arthritis with positive RA factor
  • Patients fit for parisheka swedana.

排除标准

  • Patients with systemic illness like uncontrolled diabetes mellitus, hypertension
  • Pregnant and lactating women.

结局指标

主要结局

Primary outcome will be assessed based on the following parameters

时间窗: 0th day, 07th day and 14th day

Subjective Parameters

时间窗: 0th day, 07th day and 14th day

Pain, Visual Analogue Scale, Verbal Rating Scale, Numerical Rating Scale, painDETECT,Symptoms of Rheumatoid Arthritis

时间窗: 0th day, 07th day and 14th day

Objective Parameters

时间窗: 0th day, 07th day and 14th day

RA factor, CRP, ESR

时间窗: 0th day, 07th day and 14th day

次要结局

  • Quality of life(0th day and 14th day)

研究者

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

Dr Nidhi Nirmal

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

研究点 (1)

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