CTRI/2023/11/060046尚未招募Unknown
To study the Safety and Efficacy of classical Ayurvedic treatment in the functional improvements ofpatients with Cervical Spondylitis - Nil
Mprex Healthcare Pvt.Ltd. Wakad, pune0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
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
- •1. Patients suffering from a pathological condition like a Bone tumor, Tuberculosis spine, etc.
- •2. History of injury to the cervical spine with the major surgical intervention will be excluded.
- •3. Female subjects, who are pregnant, breastfeeding, or planning to become pregnant.
- •4. Patients who are unable to walk without support and/or confined to a wheelchair or bedridden.
- •5. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
研究者
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