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临床试验/NCT06301152
NCT06301152已完成不适用

Comparison of High Intensive Laser Therapy and Extracorporeal Shock Wave Therapy in Treatment of Lateral Epicondylitis: A Randomized Controlled Study

Ankara City Hospital Bilkent2 个研究点 分布在 2 个国家目标入组 40 人开始时间: 2022年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Visual analog scale

研究概览

简要总结

Objectives: This study aims to evaluate and compare the short-term efficacy of high-intensity laser therapy (HILT) and extra corporeal shock wave therapy(ESWT) on pain, sensitivity, handgrip strength, and functions in the treatment of lateral epicondylitis (LE).

Material and methods: Forty five participants (age range, 18 to 65 years) with unilateral elbow pain were randomized into two groups. HILT group (n = 22) and the ESWT group (n = 23). The HILT and ESWT were administered three times a week for three weeks, and each treatment was combined with exercises. All patients in both groups were evaluated with ultrasonography for common extensor tendon(CET) thickness. A visual analog scale (VAS), Quick Disabilities of the Arm, Shoulder, and Hand (QDASH), and hand grip strength test were used to evaluate the patients before, one, and six weeks after treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of Lateral epicondylitis

排除标准

  • Operation history about elbow
  • Received physical therapy, or had a steroid injection to the elbow in the three months
  • Cervical radiculopathy,
  • Elbow deformities,
  • Fibromyalgia syndrome,
  • Carpal tunnel syndrome,
  • Neurological impairments in the upper extremity,
  • Chronic inflammatory conditions,
  • Hemophilia,
  • Pregnant,
  • History of malignancy

研究组 & 干预措施

high intensive laser

Experimental

high-intensity laser was applied 3 times in a week, for three weeks, total of 9 sessions

干预措施: high intensive laser (Device)

extracorporeal shock wave therapy

Experimental

extracorporeal shock wave therapy was applied once a week, for three weeks total of 3 sessions

干预措施: extracorporeal shock wave therapy (Device)

结局指标

主要结局

Visual analog scale

时间窗: Baseline, 1 week and 6 weeks

score 0-10, 0 minimum value, mean is no pain, score 10 is maximum value, pain is very severe

次要结局

  • Quick Disability Arm, Shoulder and Hand questionary,(Baseline, 1 week and 6 weeks)
  • hand grip strength(Baseline, 1 week and 6 weeks)
  • musculoskeletal ultrasonography(Baseline, 1 week and 6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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