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临床试验/CTRI/2025/09/095489
CTRI/2025/09/095489尚未招募不适用

A Comparative Clinical Evaluation Of Nimbapatradi Dhoopana And Jatyadi Taila Dressing In Dushta Vrana.

Rina Gupta1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年10月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
SUBJECTIVE

研究概览

简要总结

This is a comparative clinical study to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing in comparision to only Jatyadi Taila dressing as Jatyadi Taila is already established treatment in the Dushta Vrana, Dagdha Vrana, Sadhyo Vrana and to evaluate the efficacy of Dhoopan Karma with Jatyadi Taila dressing and only Jatyadi taila dressing in Dushta Vrana treatment. For the present research study total 40 patients are selected for clinical trial. In this clinical study, Dhoopan Karma with Jatyadi Taila dressing and only Jatyadi taila dressing will be done on 20-20 patients respectively. Patient will randomly selected with clinical features of Dushta Vrana attending the OPD and IPD of Shalya Tantra dept. and other dept. of Quadra Hospital irrespective of their gender, race, religion, occupation. This clinical study will be conducted with aim and objective to provide better, safe and effective management to the patient of Dushta Vrana. A detailed performa will be prepared on the basis of Ayurvedic text and allied Sciences. The patient fulfilling the inclusion and exclusion criteria will be registered on this performa and scoring of the different clinical features will be done on the assessment criteria. The observation of the patients will be done before, during and the after completion of trial. Little 

addition or exclusion may be done as per the necessity of the study.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

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

入选标准

  • 1 Classical signs and symptoms of Dushta Vrana irrespective of their age, sex, occupation.
  • 2 Patient between the age group of 20-70 years.
  • 3 Patient voluntary willing to participate in the clinical trial.

排除标准

  • 1 Patients of uncontrolled DM and HTN.
  • 2 Patient with any systemic disorder.
  • 3 Patient with any Anatomical abnormalities.
  • 4 Pregnant and Lactating mothers 5 HIV/HCV/HBsAG positive patient.

结局指标

主要结局

SUBJECTIVE

时间窗: Assessment will be carried out on intermittent days of 4 week i.e. on 0th, 7th, 14th, 21st, 28th day to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing And only Jatyadi Taila dressing in Dushta Vrana.

The assessment of trial will be done based on improvement in the symptoms mentioned as-

时间窗: Assessment will be carried out on intermittent days of 4 week i.e. on 0th, 7th, 14th, 21st, 28th day to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing And only Jatyadi Taila dressing in Dushta Vrana.

1- Vedana (Pain)

时间窗: Assessment will be carried out on intermittent days of 4 week i.e. on 0th, 7th, 14th, 21st, 28th day to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing And only Jatyadi Taila dressing in Dushta Vrana.

2- Daha (Burning Sensation)

时间窗: Assessment will be carried out on intermittent days of 4 week i.e. on 0th, 7th, 14th, 21st, 28th day to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing And only Jatyadi Taila dressing in Dushta Vrana.

3- Kandu (Itching)

时间窗: Assessment will be carried out on intermittent days of 4 week i.e. on 0th, 7th, 14th, 21st, 28th day to find out the efficacy of Dhoopan Karma with Jatyadi Taila dressing And only Jatyadi Taila dressing in Dushta Vrana.

次要结局

  • Objective(1) Tenderness)

研究者

发起方
Rina Gupta
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Rina Gupta

Quadra Institute Of Ayurveda

研究点 (1)

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