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临床试验/NCT03596203
NCT03596203已完成1 期

TransCutaneous Magnetic Stimulation (TCMS) for the Treatment of Foot Pain Caused By Diabetic Neuropathy

University of Maryland, Baltimore2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2018年11月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
17
试验地点
2
主要终点
Pain level

研究概览

简要总结

The study will evaluate whether an experimental medical device that emits a series of brief, intense magnetic pulse will relieve foot pain from Diabetic Neuropathy (DN). The United States Food and Drug Administration (FDA) has approved a similar device for treatment of migraine headaches, but this type of device has not been studied for the treatment of DN.

详细描述

The study will evaluate whether an experimental medical device that emits a series of brief, intense magnetic pulse will relieve foot pain from Diabetic Neuropathy (DN). The United States Food and Drug Administration (FDA) has approved a similar device for treatment of migraine headaches, but this type of device has not been studied for the treatment of DN. No significant adverse reactions or side effects have been reported from the use of magnetic stimulation for the headache treatment. Some patients who have migraine headaches have excellent pain relief with the magnetic treatment even if they did not get pain relief using medications.

The investigators do not know whether this magnetic treatment will relieve the foot pain caused by diabetic neuropathy, so they will test this by applying 50 strong magnet pulses to the painful area of each foot. This procedure will be repeated onto three parts of each foot. First onto the bottom of the foot, then the top of the foot and then the back of the foot including a portion of the ankle. The effect on pain in each foot while walking for about 10 steps will be recorded before the study begins and periodically for 28 days. This testing will provide data as to any improvement in pain relief. If the participants' reported pain is reduced as a result of the magnetic treatment, then the magnetic pulses will have shown that they have reduced the pain. Additional studies will be needed to further investigate this treatment and to determine how to obtain statistically significant data as to whether this therapy reduces the foot pain caused by diabetic neuropathy.

One side effect of this treatment may be some muscular jerking of the foot or the leg during the application of the magnetic pulses. This jerking will last only during the treatment and will not be painful or harmful.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years of age.
  • Prescription pharmacologic treatment is insufficient for treatment of pain.
  • Pain duration of more than one months.
  • Pain occurs daily.
  • Chronic DN associated pain that is located in bilateral feet and is not explained by a central anatomic nerve compression and can clearly be correlated with that patient's history of diabetes.
  • Pain intensity ≥ 5 in each foot at the time of enrollment.

排除标准

  • Life expectancy ≤ 6 months.
  • Oral pain medication doses or active ingredient has changed significantly in the prior 2 weeks.
  • Inability to walk at least 10 steps (with or without a cane) before and after having to sit in a chair.
  • Another pain condition that might confound results (e.g., neuropathy from cancer chemotherapy).
  • Inability to undergo study assessments or complete questionnaires independently.
  • Active psychological co-morbidities (i.e., uncontrolled schizophrenia)
  • Currently using an opioid medication for the treatment of foot pain.

结局指标

主要结局

Pain level

时间窗: 1 to 28 days

Numeric Pain Rating Scale, 0-10 with 0 being no pain, and 10 being worst pain ever experienced

次要结局

  • Functional status and Patient satisfaction with treatment(1 to 28 days)
  • Changes in pain medication(1 to 28 days)

研究者

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

Kashif Munir

Associate Professor

University of Maryland, Baltimore

研究点 (2)

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