跳至主要内容
临床试验/KCT0000506
KCT0000506招募中未知

Electroacupuncture for Chemotherapy-induced Peripheral Neuropathy: A Randomized, Patient-Assessor Blinded, Controlled Pilot Clinical Trial

Korea Institute of Oriental Medicine0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
18(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. Males and females aged 18 years and older
  • 2. Patients who had received or were currently receiving neurotoxic chemotherapy with a diagnosis of cancer
  • 3. Symptoms of peripheral neuropathy of duration = 1 month attributed to chemotherapy, and a score = 4 out of 10 on the NRS scale.
  • 4. No use of medications to prevent or treat neuropathy within 2 weeks or stable use had been made in their medications to prevent or treat neuropathy within 2 months before screening.
  • 5. ECOG PS of 0-2
  • 6. Life expectancy = 6 months
  • 7. Agreed with written informed consent

排除标准

  • 1. Pre-existing or history of peripheral neuropathy due to any cause other than chemotherapy (diabetes, peripheral vascular disease, HIV, alcohol, toxin, hereditary, nerve compression injuries, etc.)
  • 2.Known hypersensitivity reaction after acupuncture treatment or inability to cooperate with acupuncture procedure
  • 3. Received acupuncture, moxibustion, cupping or herbal medicine for peripheral neuropathy last 4 weeks
  • 4. Cardiovascular disorder (e.g. arrhythmia) or using pacemaker
  • 5. Pregnant, expecting pregnant or nursing women
  • 6. Those who are not willing to comply with this study protocol

研究者

相似试验

Electroacupuncture for Chemotherapy-induced... | 临床试验