A PRECLINICAL AND COMPARATIVE CLINICAL TRIAL OF VARMAM THERAPY WITH AND WITHOUT KURUNTHOTTI KASHAYAM (INTERNALLY) IN THE MANAGEMENT OF CEGANAVATHAM (CERVICAL SPONDYLOSIS)

National Institute of Siddha1 个研究点分布在 1 个国家目标入组 40 人开始时间: 2020年11月29日最近更新: 2020年11月22日

适应症

试验速览

阶段: 3 期
状态: 尚未招募
发起方: National Institute of Siddha
入组人数: 40
试验地点: 1
主要终点: UNIVERSAL PAIN ASSESSMENT SCALE

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This is the comparative two arm clinical study to evaluate the efficacy of varmam therapy with and without kurunthotti kashayam in the management of ceganavatham in 40 patients for 48 days. The outcome will be measured by Universal pain scale and reduction in clinical symptoms.

研究设计

研究类型: Interventional
分配方式: Computer generated randomization

入排标准

年龄范围: 25.00 Year(s) 至 55.00 Year(s)（—）
性别: All

入选标准

•Pain present behind the neck Region, aggravated by movement
•Neck stiffness
•Difficulty in flexion and extension of neck 4.pain radiating to shoulder blade, top of the shoulder, upper arm and back of the head
•Dizziness or vertigo
•Numbness in both upper limb
•Pain radiating to.

排除标准

•Patient with uncontrolled hypertension 2.pregancy and lactation
•Cervical rib
•Spina bifida
•Ankylosis spondylosis
•Rheumatoid arthritis
•Patient with thyroid
•Any trauma history
•Loss of bowel and bladder control
•Dysphagia
•Fracture in neck region
•Coronary artery disease
•Tuberculosis
•Severe osteoporosis
•Neck surgery.

结局指标

主要结局

UNIVERSAL PAIN ASSESSMENT SCALE

时间窗: 48 days

次要结局

To study the siddha basic principles relevant to the diseases(48 days)

研究者

发起方

National Institute of Siddha

申办方类型

Research institution and hospital

研究点 (1)

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