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临床试验/NCT05846958
NCT05846958招募中不适用

Efficacy of Laser Acupuncture on Neurophysiological Parameters of Median Nerve in Postpartum Women: A Randomized Controlled Clinical Trial

Cairo University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
sensory nerve conduction velocity (SNCV) measured in m/s

研究概览

简要总结

BACKGROUND: Carpal tunnel syndrome (CTS), the most common entrapment neuropathy of the upper extremity, is caused by compression of the median nerve as it travels through the carpal tunnel CTs is a very common complication found in pregnancy, which is reported as high as 62% in pregnant females. The functioning of median nerve is compromised in almost all pregnant females especially during the third trimester of pregnancy, the majority may still feel some symptoms up to 3 years after delivery. Many clinicians have used LLLT on acupuncture points, which is called laser acupuncture (LA), to treat many clinical problems, such as musculoskeletal pain, lateral epicondylitis, headaches, etc. In contrast with traditional acupuncture needles, LA is a non-invasive therapy that does not cause tingling/pain during procedures Objective: to determine efficacy of laser acupuncture on electrophysiological parameters of median nerve in postpartum women

详细描述

Intervention description

  1. Experimental Group:

Each patient in this group will receive laser acupuncture on PC4 (Ximen), PC6 (Neiguan), PC7 (Daling), PC8 (Laogong), LI4 (Hegu), LI10 (Shousanli), LI11 (Quchi), HT3 (Shaohai), HT7 (Shenmen), LU10 (Yuji) acupoints in addition to wearing night splint. LA will be applied to each acupuncture point for 10 s with at least 4J/points based on the recommended LLLT treatment doses for CTS of the World Association of Laser Therapy. 2. Control Group:

Each patient in this group will wear night splint every night for 4 weeks

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
25 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Their BMI will be range from 25 to 30 Kg/m
  • The electrophysiological evidence of mild or moderate median nerve lesion at wrist (mild: sensory nerve latency >3.5 ms at third digit, moderate: sensory nerve latency >3.5 ms at third digit and median motor latency>4.2 ms)
  • Positive phalen's test.
  • Positive tinel's test.
  • Carpal tunnel of dominant hand could be participated.

排除标准

  • History of brachial plexopathy or malignancy.
  • Radial, ulnar neuropathy, proximal median neuropathy or polyneuropathy.
  • Previous wrist surgery or steroid injection for carpal tunnel syndrome.
  • History of trauma, fracture, deformity or inflammation in the wrist, such as rheumatoid arthritis.
  • Coagulation abnormalities, pregnancy, fever and infections.
  • Skin disease and skin cancer.
  • Spots, birthmarks or tattoos over the work points. 8- Pacemaker and implementable medical devices.

结局指标

主要结局

sensory nerve conduction velocity (SNCV) measured in m/s

时间窗: 4 weeks

will be measured at the beginning of the study and at the end of the treatment program througth EMG

次要结局

  • Hand grip strength in Kg(4 weeks)
  • Symptoms severity and functional capacity (Score)(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Afaf Mohamed Botla

Principal investigator

Cairo University

研究点 (2)

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