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临床试验/NL-OMON44713
NL-OMON44713已完成不适用

Meralgia Paresthetica, locating the lateral femoral cutaneous nerve (LFCN) with elektro-stimulation followed by a therapeutic injection of methylprednisolone/lidocaïne (M/L), a double-blind randomized placebo-controlled clinical trial - Meralgia Paresthetica Elektrostimulation Study

HagaZiekenhuis0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
20

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 至 64(—)

入选标准

  • Adult patients with newly diagnosed idiopathic meralgia paresthetica will be recruited. Age: 18 years and older. Duration 4 weeks or more.
  • Diagnostic criteria: Meralgia paresthetica characterized by pain, numbness and tingling in the anterolateral aspect of the thigh in the area of the LFCN

排除标准

  • 1. Coexisting disorders or conditions that may mimic MP such as lumbar radiculopathy, severe polyneuropathy.
  • 2. Known allergic reaction to methylprednisolone/lidocaine.
  • 3. Pregnancy
  • 4. No localization possible through electrostimulation
  • 5. Systemic viral or fungal infections
  • 6. Known allergy to steroids
  • 7. No injection with steroids can be given in a vicinity of a preexistent infectious area

研究者

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