ChiCTR1800017905招募中1 期
COMPARISON OF EFFECTIVENESS OF MEDIAN NERVE NEURODYNAMIC MOBILIZATION VERSUS CARPAL BONE MOBILIZATION ON PAIN, SYMPTOM SEVERITY AND FUNCTIONAL STATUS IN CARPAL TUNNEL SYNDROME
Self Financed2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年8月1日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Boston Carpal Tunnel Questionnaire
研究概览
简要总结
To determine the effectiveness of median nerve mobilization vs. carpal bone mobilization in reducing pain & symptom severity and improving functional status in subjects with carpal tunnel syndrome
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
入排标准
- 年龄范围
- 25 至 55（—）
- 性别
- All
入选标准
- •Age 25-55 years.
- •Both male and female patients diagnosed with CTS;
- •Patients with positive phalen's test, positive tinel's test and positive upper limb tension test for median nerve;
- •Patient's having median nerve latencies above 4ms.
排除标准
- •Any red flags (tumor, fracture, metabolic diseases, rheumatoid arthritis, osteoporosis,HTN, prolonged history of steroid use, etc);
- •Patients with double crush syndrome, cervical or thoracic origin of symptoms, scaphoid instability, shoulder injuries, recent fractures and crush injuries, hypermobile joints, pregnancy and women undergoing hormone replacement therapy;
- •Evidence of central nervous system involvement;
- •Patients who requested to leave the study and history of other treatments including local corticosteroid and using of physical modalities and physiotherapy injection and splint in 3 months ago;
- •Any sensory and/or motor deficit in either ulnar or radial nerve.
研究组 & 干预措施
Group 1
Carpal Bone Mobilization
Group 2
Median Nerve Neurodynamic Mobilization
结局指标
主要结局
Boston Carpal Tunnel Questionnaire
时间窗: Pretreatment, after 3 weeks, after 6 weeks
Numeric rating pain scale
时间窗: Pretreatment, after 3 weeks, after 6 weeks
次要结局
未报告次要终点
研究者
研究点 (2)
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