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临床试验/CTRI/2023/02/049879
CTRI/2023/02/049879招募中2 期

A single arm clinical study to evaluate the efficacy of Punarnavadi Upanaha Sweda in the management of Janusandhigatavata.

Dr.Pooja Bondge1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2023年1月4日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
32
试验地点
1
主要终点
To assess the efficacy of Punarnavadi Upanaha Sweda in the pain reduction of Janusandhigatavata using VAS scale

研究概览

简要总结

It is the clinical study to evaluate the effect of punarnavadi upanah sweda in the management of Janusandhijatavata.

Study design is single arm  clinical study.

Total 32 patients will be enrolled .

Assesment of patients  1ST ,7TH Day.

Follow up on  14 th day.

Total duration of study will be 18 months.

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 80.00 Year(s)(—)
性别
All

入选标准

  • Patients in age group of 18 to 80 yrs.
  • Patient of Janusandhigatavata having classical signs & symptoms like shool(joint pain), shoth(joint swelling),akunchan prasaran kashtata(pain during movements) (ch.chi.28/37).

排除标准

  • Patient with other joint disorders such as k/c/o Amavata & Vatarakta.
  • k/c/o Auto immune Diseases-Ankylosing Spondylitis k/c/o Neoplasm.
  • Permanent joint Damage.

结局指标

主要结局

To assess the efficacy of Punarnavadi Upanaha Sweda in the pain reduction of Janusandhigatavata using VAS scale

时间窗: 14 days

次要结局

  • To assess the efficacy of Punarnavadi Upanaha sweda in the management of joint restriction of Janusandhigatavata using goniometric measurement.

研究者

发起方
Dr.Pooja Bondge
申办方类型
Other [self]

研究点 (1)

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