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临床试验/CTRI/2024/10/074794
CTRI/2024/10/074794尚未招募2 期

A comparative clinical evaluation of Virechana Karma with Kashmaryadi Kashaya and Eranda Taila in Vatarakta(Gouty Arthritis)

Patanjali Bhartiya Ayurvigyan Evum Anusandhan Sansthan1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年10月11日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
3. Svathu (Swelling)

研究概览

简要总结

This study is a Comparative Clinical evaluation of Virechana Karma with Kashmaryadi Kasahaya and Eranda Taila in Vatarakata (Gouty Arthritis)

This will be conducted on 40 randomly selected patients from Opd/Ipd of Panchakarma department of Patanjali Bhartiya Ayurvigyan evum Anusandhan Sansthan Haridwar. patient will be divided into 2 groups - 20 patients will be administered Kashmaryadi Kashaya for Virechana and 20 patients will be administered with Eranda Taila for Virechana. Follow up will be taken after 1 month assessment to be done on the basis of subjective and objective parameters as discussed earlier.

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 60.00 Year(s)(—)
性别
All

入选标准

  • Patient present with clinical features of Vatarakta.
  • 1.Patient of either sex between age group of 18 to 60 years.
  • 2.Patients were selected irrespective of sex, occupation, socio economic status, religion etc.
  • Patient fit for Virechana Karma.
  • Patient showing uric acid level above 7mg/dl.

排除标准

  • Patients below the age of 18 years and above 60 years were excluded.
  • Patient with metabolic disorder, hypertension, systemic disorders, autoimmune diseases, any endocrine disorder and any other malignancy.
  • Patient with infection and communicable disease.
  • Patients who are pregnant and lactating mother.
  • Patient associated with Rheumatoid arthritis, osteoarthritis.
  • Patient with anorectal diseases like fistula and hemorrhoids.

结局指标

主要结局

3. Svathu (Swelling)

时间窗: 10,30 days

1. Arti (Pain)

时间窗: 10,30 days

2. Stabhdhata (Stiffness)

时间窗: 10,30 days

4. Daha (Burning)

时间窗: 10,30 days

5. Vaivarnya (Discoloration)

时间窗: 10,30 days

次要结局

  • Objective parameter(1. CBC with ESR)

研究者

发起方
Patanjali Bhartiya Ayurvigyan Evum Anusandhan Sansthan
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Akansha Singh

Patanjali Bhartiya Ayurvigyan Evum Anusandhan Sansthan Haridwar Uttarakhand

研究点 (1)

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