跳至主要内容
临床试验/CTRI/2023/02/049531
CTRI/2023/02/049531已完成不适用

Comparative Study of Panchdhatu Shalaka vesus Sneha dagdha in the Management of Kadar w.s.r. to Corn

Dept Of Shalya Tantra1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年12月15日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
3. MIld improved-25-50% relief in sign and symptoms.

研究概览

简要总结

A minimum of 60 patients suffering from Kadar in group of 30 patients will be selected for the study. A special proforma will be prepared with detailed history and sign and symptoms as mentioned in our classics and allied science. Patients will be analyzed and selected accordingly.  Agnikarma of selected patients will be carried out on the day of registration and after the resolution of the symptoms of the same patient after the period of 7 days.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients of age 20-60yrs.
  • 2.Patients having hyperkeratosis lesions/ Kadar.
  • 3.Kadar present in Pada tala and hasta tala.

排除标准

  • 1.Patients contra-indicated for Agnikarma.
  • 2.Patients having any serious systemic disease.
  • 3.Pregnant women, lactating women and children and people aged below 20 years and above 60 years.
  • 4.Infected Corns & having more than 3-4 Kadar.
  • 5.Those who are psychologically not fit for the treatment.
  • 7.Patients who are known case of HTN, DM, Tuberculosis etc.

结局指标

主要结局

3. MIld improved-25-50% relief in sign and symptoms.

时间窗: 4 weeks with 4 weeks of followup.

4.No improvement- less tham 25% relief in sign and symptoms.

时间窗: 4 weeks with 4 weeks of followup.

1. Mrked improved- More then 75% relief in sign and symptoms.

时间窗: 4 weeks with 4 weeks of followup.

2.Moderate improved- 50- 75% relief in sign and symptoms.

时间窗: 4 weeks with 4 weeks of followup.

次要结局

  • To improve in quality of life(SF-36).(4 weeks with 4 weeks of follow up.)

研究者

发起方
Dept Of Shalya Tantra
申办方类型
Government medical college

研究点 (1)

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