CTRI/2020/07/026778已完成2 期
An open labelled double arm non randomised phase II clinical trial to compare the efficacy of VARMA MANIPULATION with KUTHIKAAL VATHA KUDINEER (internal)and NOCHI ILAI KATTU(external)in the treatment of KUTHIKAAL VATHAM
Government siddha medical college and hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年7月24日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Assessment of change from baseline in Universal Pain Assessment scale at day 48 between GroupI(Varma therapy)and GropII(Medicine and Varma therapy) comparison of efficacy in patient GroupI and GroupII
研究概览
简要总结
calcneal spurl -the spike of bone at the anterior edge of the calcanum on the medial aspect is otherwise calcaneal spur.According to siddha text the sgn and symptoms of kuthikaal vatham is correlated with calcaneal spur. This study is evaluate the efficacy of varma manipulation and cilnical efficacy of kuthikaal vatha kudineerinternal)nohi ilai kattu (external). The manipulation of varma points for treating disease called varma therapy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •patient having symptoms of sharp pain like knife in the heel when standing up in the morning ,a dull ache in the heel throughout the rest of the day patient who are willing to give radiological investigation and provide blood for lap invetigation patient willing to sign the informed consent stating that he/she will conscientiously sick to the treatment during 48 days but can option out of the trial of his/her own conscious giscretion.
排除标准
- •fracture of the foot ,pagets disease affecting the calcanium,rupture of Achilles tendon,systemic disorder like TB,DM,HIV,Leukaemia.
结局指标
主要结局
Assessment of change from baseline in Universal Pain Assessment scale at day 48 between GroupI(Varma therapy)and GropII(Medicine and Varma therapy) comparison of efficacy in patient GroupI and GroupII
时间窗: 48 days
次要结局
- Assessment of quality of life by Universal Pain score scale.Assessment of safety parameters(48 days)
研究者
研究点 (1)
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