A Comparative Clinical Study Of Agnikarma And Viddhakarma In Greeva Hundanam
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 revalidate the efficacy of Viddhkarma as Anubhut Chikitsha Prayog in comparison to Agnikarma as Agnikarma is already established treatment in the pain management and to evaluate the efficacy of Agnikarma and Viddhkarma as SadyaShoolHar Chikitsha. For the present research study total 40 patients are selected for clinical trial. In this clinical study, Viddhkarma and Agnikarma will be done on 20-20 patients respectively. Patients will randomly selected with clinical features of GreevaHundanam 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 GreevaHundanam. A detailed performa will be prepared on the basis of Ayurvedic text and allied Sciences. The patient fullfiling 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
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1 Classical signs and symptoms of GreevaHundanam irrespective of their age,sex,occupation.
- •2 Patients between the age group of 18-60 years.
- •3 Patient voluntary willing to participate in the Clinical trial.
- •4 X-Ray showing radio logical signs for Cervical Spondylosis.
排除标准
- •1 Patients of RA, Musculoskeletal disorder other than Greeva Hundanam.
- •2 Patients of uncontrolled DM and HTN.
- •4 Patients with any Anatomical abnormalities.
- •5 Pregnant and Lactating mothers.
结局指标
主要结局
SUBJECTIVE
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
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 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
1) Neck pain (GreevaShool).
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
2) Pricking sensation.
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
3) Stiffness (GreevaStambha).
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
4) Heaviness.
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
5) Vertigo (Bhrama)
时间窗: • Assessment will be carried out on intermittent days of 1 week i.e – on 1, 3, 5, 7 day to find out the efficacy of Agnikarma and Viddhakarma in Greeva Hundanam.
次要结局
- OBJECTIVE(1) Range of Motion.)
研究者
Laxmi Dixit
Quadra Institute of Ayurveda and Hospital