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临床试验/CTRI/2025/02/079977
CTRI/2025/02/079977尚未招募2/3 期

A Pragmatic comparative clinical trial to evaluate effectiveness of topical application of Jiraka Ghrta against Yashtimadhuadi Ghrta in Agnidagdha Vrana after Corn excision

VPSV Ayurveda College Kottakkal1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月15日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
3. Pain by using Visual Analogue Scale

研究概览

简要总结

A pragmatic  trial is planned in Corn (Kadara) after excision and agnikarma to heal the wound by comparing Yashtimadhuadi ghrta and Jeeraka ghrta. Burns are very common and has the global prevalence of 6-7 million per year. There are so many medicines in Ayurveda which are beneficial in treating burns. One such yoga mentioned in Susruta samhita sutrasthana Agnikarma vidhi is Yashtimadhuadi ghrta. It contains 8 drugs having the property of RopanÌ£a. There are simple formulations available in the latterly evolved classical Ayurvedic books, which are found to be effective in clinical practice but not yet scientifically validated.  JiÌ„raka GhrÌ£ta is a formulation explained in the context of AgnidagdhavranÌ£a CikitsaÌ„dhikaÌ„ra consisting of easily available drugs like JiÌ„raka, Sarjarasa and MadhuÌ„cchisÌ£tÌ£a which can be easily prepared. This study  will be done in 15 participants in each group for a period of 14 days, in the age group of 21-70 years. Participants diagnosed as per diagnostic criteria and satisfying inclusion criteria will be selected consecutively into 2 groups from the OPD of VPSV Ayurveda College Hospital, Kottakkal. After Agnikarma, Group 1 participants will be dressed with JiÌ„raka GhrÌ£ta, and Group 2 participants will be dressed with YasÌ£tÌ£iÌ„madhuaÌ„di GhrÌ£ta once in alternative days up to 14 days. Assessment will be done on subjective parameters like pain and burning sensation and objective parameters like size of wound and discharge. Data will be analysed using appropriate Statistical tests.

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
21.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1.Subjects with informed consent.
  • 2.Subjects satisfying diagnostic criteria.

排除标准

  • 1.Subjects having difficulty in reaching OPD on alternative days will be excluded.

结局指标

主要结局

3. Pain by using Visual Analogue Scale

时间窗: 0th 6th and 14th day

1.Size of the wound- Diameter and depth

时间窗: 0th 6th and 14th day

2. Discharge from wound

时间窗: 0th 6th and 14th day

次要结局

未报告次要终点

研究者

发起方
VPSV Ayurveda College Kottakkal
申办方类型
Other [[Aided College]]
责任方
Principal Investigator
主要研究者

Dr Ajith Narayanan A M

VPSV Ayurveda college Kottakkal

研究点 (1)

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