KCT0003883已完成未知
To evaluate the efficacy and safety of the newly developed low-intensity ultrasound-transcutaneous nerve stimulation combined therapy for knee pain with osteoarthritis for 20 minutes, 3 times a day (more than 10 times a week) for a total of 8 weeks Single-institution, double-blind, randomized, parallel design, study-based clinical trials
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- 19(Year) 至 65(Year)(—)
- 性别
- All
入选标准
- •1) Adults aged 19 and over, under 65 years of age
- •2) who were diagnosed with Kellgren-Lawrence (K-L) scale on anteroposterior plane radiograph of the knee in standing posture
- •3) Those who fully understand the purpose of the research and wish to participate in the clinical research through voluntary consent
排除标准
- •1) Those who do not meet the age criteria
- •2) Persons suspected of having neurological disorders on physical examination
- •3) Those who appeal for sensory depression
- •4) Those who underwent knee surgery within the last 6 months
- •5) Those who have undergone lower limb surgery and cortisone injections treatment within the past month (including steroids, nonsteroidal anti-inflammatory drugs, etc.)
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