To study the Safety and Efficacy of classical Ayurvedic treatment in the functional improvements ofpatients with Cervical Spondylitis
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- other associated symptoms
研究概览
简要总结
Cervical spondylosis is a general term affecting the spinal disc in the neck. The inter-vertebral spaces are affected most and start at the degeneration of discs resulting in a reduction of inter-vertebral disc space. It develops restricted cervical spine movement in the neck due to pain and swelling. The study aims to assess the Safety and Efficacy of classical Ayurvedic treatment in the functional improvements of patients with Cervical Spondylitis. The therapeutic effect is assessed by comparing relief from stiffness and other associated symptoms. Adverse effects reported by patients during treatment will be recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 30.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Male and female subjects 30-60 years of age (both inclusive) 2.Subject diagnosed with cervical spondylitis with or without nerve compression for more than three months.
- •3.Pain in the neck and shoulder, and difficulty with neckline rotation, flexion, extension,etc.
- •4.Subject have Muscle spasm, Numbness, Tingling sensation, and joint stiffness.
- •5.Be willing to refrain from taking analgesics, anti-inflammatory agents, corticosteroids, muscle relaxants, etc.
- •during the entire trial.
- •6.An ambulatory subject can provide verbal and written consent and is ready to comply with all study procedures.
排除标准
- •Patients suffering from a pathological condition like a Bone tumor, Tuberculosis spine, etc.
- •History of injury to the cervical spine with the major surgical intervention will be excluded.
- •Female subjects, who are pregnant, breastfeeding, or planning to become pregnant.
- •Patients who are unable to walk without support and/or confined to a wheelchair or bedridden.
- •History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
结局指标
主要结局
other associated symptoms
时间窗: Seven Sessions in two weeks
2. To study the patient’s relief from stiffness &
时间窗: Seven Sessions in two weeks
1. To study Panchakarma Essentials efficacy in
时间窗: Seven Sessions in two weeks
reducing cervical spondylitis pain.
时间窗: Seven Sessions in two weeks
次要结局
- 1. To study improvement in the Cervical Range(of Movement.)