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临床试验/NCT05863546
NCT05863546已完成不适用

Effect of Different Doses of Therapeutic Ultrasound in the Treatment of Carpal Tunnel Syndrome

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年9月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
symptoms severity and functional status

研究概览

简要总结

The purpose of this study was to investigate the effective dose of therapeutic ultrasound in the treatment of carpal tunnel syndrome on pain level, functional ability, motor and sensory nerve conduction parameters and pinch strength.

详细描述

Carpal tunnel syndrome (CTS) is among the most common peripheral neuropathies causing the median nerve compression as it crosses the carpal tunnel, with an estimated prevalence of about 4 - 5% of the general population. Patients suffering from this syndrome mainly complain about paresthesia (pain, numbness, and tingling) in the innervation area of the median nerve in the hand which could be accompanied by weakness and atrophy of thenar muscles.

Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy of the upper limb and a significant contributor to hand functional impairment and disability that could be treated through numerous approaches. Effective treatment options include conservative and surgical interventions.

Carpal Tunnel Syndrome (CTS) remains a puzzling and disabling condition present in 3.8% of the general population. CTS is the most well-known and frequent form of median nerve entrapment, and accounts for 90% of all entrapment neuropathies.

Physiotherapy modalities are used to help patients with CTS in many cases. They can both help to improve CTS symptoms as well as resolve the cause of the syndrome. Physiotherapy intervention may include special exercises, mobilizations, ergonomic interventions and advice for as well as electrotherapy modalities, aiming for the treatment and improvement of symptoms.

Ultrasound waves have anti-inflammatory properties, stimulating nerve regeneration and improving nerve conductivity.

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
Single (Participant)

入排标准

年龄范围
25 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Subject's age range was 25-55 years .
  • Mild to moderate CTS, that is confirmed by neurologist or orthopedist based on results of physical examination and electrophysiological criteria; i. Mild CTS is characterized by sensory fibers involvement (sensory peak latency > 3.6 milliseconds) with no motor fiber involvement (motor distal latency < 4.1 milliseconds), provided that sensory nerve action potential (SNAP) is not absent.
  • ii. Moderate CTS is characterized by involvement of both sensory and motor fibers, provided that neither of these two waves is absent .
  • Pain intensity more than 5 in visual analogue scale (VAS).

排除标准

  • History of any trauma on the hands, neck, and shoulders within 3 months of the study onset
  • Cervical radiculopathy, peripheral polyneuropathy, or other neurological conditions.
  • Patients suffering from severe CTS according to electrophysiological criteria

结局指标

主要结局

symptoms severity and functional status

时间窗: Four weeks

Symptoms severity and functional status were measured by Boston carpal tunnel syndrome questionnaire. The patients rated their ability to perform the activity on a scale that ranged from 1 (no difficulty with the activity) to 5 (cannot perform the activity at all).

median nerve motor distal latency

时间窗: Four weeks

Electrodiagnostic tests were used to measure median nerve motor distal latency in milliseconds.

Pinch strength

时间窗: Four weeks

Pinch dynamometer was used to measure pinch strength

median nerve motor amplitude

时间窗: Four weeks

Electrodiagnostic tests were used to measure motor amplitude in millivolt.

median nerve sensory distal latency

时间窗: Four weeks

Electrodiagnostic tests were used to measure median nerve sensory distal latency in milliseconds.

median nerve sensory amplitude

时间窗: Four weeks

Electrodiagnostic tests were used to measure sensory amplitude in millivolt

Pain intensity

时间窗: Four weeks

Pain intensity was measured by visual analogue scale. Scores are based on self-reported measures of symptoms that are recorded with a single handwritten mark placed at one point along the length of a 10-cm line that represents a continuum between the two ends of the scale-"no pain" on the left end (0 cm) of the scale and the "worst pain" on the right end of the scale (10 cm).

次要结局

未报告次要终点

研究者

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

Omnia Gamal Mohamed

physical therapist

Cairo University

研究点 (1)

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