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临床试验/NCT07342426
NCT07342426招募中4 期

Comparison of the Effects of High and Low Dose High-intensity Laser Therapy in Patients With Lateral Epicondylitis

Kaohsiung Medical University Chung-Ho Memorial Hospital1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2026年1月12日最近更新:
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
45
试验地点
1
主要终点
Pain intensity

研究概览

简要总结

High-intensity laser therapy has gained increasing attention in recent years as a therapeutic modality. It is a non-invasive treatment that can reduce pain, increase local blood circulation, and promote tissue repair. The higher energy output of high-intensity laser therapy also have deeper tissue penetration. Several studies have investigated the effects of high-intensity laser therapy on lateral epicondylitis, and the existing literature indicates that, compared with other treatment modalities, high-intensity laser therapy is more effective in improving pain and quality of life in patients with lateral epicondylitis.

However, the dosage, duration, and treatment frequency applied in previous studies vary considerably. The therapeutic effects of high-intensity laser therapy may therefore be influenced by treatment dosage. Consequently, the purpose of this study is to compare the effects of two different dosages of high-intensity laser therapy on patients with lateral epicondylitis.

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
Double (Participant, Care Provider)

入排标准

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

入选标准

  • Patients diagnosed with lateral epicondylitis by physician
  • Disease duration of less than three months
  • Adults aged above 18 years with full decision-making capacity

排除标准

  • Patients who have received treatments other than standard treatment to the affected area within past three months
  • Patients with contraindication for rehabilitation therapy
  • Photosensitivity
  • Sensory impairment
  • Implanted cardiac pacemaker
  • Patients with a history of surgery on the affected elbow
  • Patients with cervical radiculopathy

研究组 & 干预措施

Conrol group

Placebo Comparator

Placebo high intensity laser therapy with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Infarred ray therapy system (Device)

Conrol group

Placebo Comparator

Placebo high intensity laser therapy with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Transcutaneous electrical nerve stimulator (Device)

Low dosage group

Experimental

Low dosage High intensity laser with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: High intensity laser therapy (Device)

Low dosage group

Experimental

Low dosage High intensity laser with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Infarred ray therapy system (Device)

Low dosage group

Experimental

Low dosage High intensity laser with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Transcutaneous electrical nerve stimulator (Device)

High dosage group

Experimental

High dosage High intensity laser therapy with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: High intensity laser therapy (Device)

High dosage group

Experimental

High dosage High intensity laser therapy with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Infarred ray therapy system (Device)

High dosage group

Experimental

High dosage High intensity laser therapy with Infarred ray and Transcutaneous electrical nerve stimulator therapy

干预措施: Transcutaneous electrical nerve stimulator (Device)

结局指标

主要结局

Pain intensity

时间窗: From enrollment to the end of treatment at 4 weeks

Using visual analog scale to measure pain intensity

次要结局

  • Grip strength(From enrollment to the end of treatment at 4 weeks)
  • Quality of life(From enrollment to the end of treatment at 4 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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