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临床试验/IRCT2014052811341N2
IRCT2014052811341N2已完成未知

Comparison of effectiveness of topical chamomile oil and placebo in the advancement of Boston questionnaire's score and electrodiagnostic criteria of patients with mild and moderate carpal tunnel syndrome

Shiraz University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 70 years(—)
性别
All

入选标准

  • primary idiopathic carpal tunnel syndrome; patients aged between 18-70 years old; electrodiagnostic criteria for mild or moderate CTS; Patient's written informed consent for inclusion; having at least two signs or one sign plus one symptom of: paresthesias, numbness, tingling, night pain positive Phalen test, positive Tinnel test, positive compression test. Exclusion criteria: Clinical and electrodiagnostic evidence of severe CTS including muscular atrophy and neurogenic changes in needle EMG of APB muscle; recurrent carpal tunnel syndrome; Positive history of trauma and/or fracture of wrist bones and/or surgical release of median nerve and/or direct injection into carpal tunnel of wrist; Evidence of cervical radiculopathy in EMG; Systemic disease including: neuropathies (rule out by nerve conduction study of ulnar nerves) and/or collagen vascular diseases such as SLE and scleroderma and RA; Endocrine diseases such as hypothyroidism and DM; Other disease-inducing neuropathy; Situations such as renal failure and/or alcoholism and/or poor medical condition; History of recent and ongoing use of corticosteroids or analgesics that could not be discontinued; hypersensitivity to the drug or placebo; inability to completion of data gathering forms (cognitive or language disorder).

排除标准

  • 未提供

研究者

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