NCT06982989招募中不适用
Clinical Study on the Treatment of Pelvic Pain With Wearable Dual-band LED Device
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 250
- 试验地点
- 1
- 主要终点
- Efficacy that LED release pelvic pain
研究概览
简要总结
This study is a prospective clinical trial, which intends to prospective include female pelvic pain (dysmenorrhea and chronic pelvic pain), screen suitable cases, wear dual-band LED devices in non-menstrual period, perform low-dose phototherapy on local pelvic area and acupoints, and observe the changes of pelvic pain and related serological indicators in clinical practice.
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 35 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •pelvic pain
排除标准
- •Irregular menstrual cycles;
- •Inflammatory disease;
- •pregnant;
- •Light allergy;
研究组 & 干预措施
Use LED to treat pelvic pain
Other
patient choose LED to treat pelvic pain
干预措施: use LED to treat pelvic pain (Device)
结局指标
主要结局
Efficacy that LED release pelvic pain
时间窗: 1 month after the treatment
Use VAS scale to evaluate the pain.The changes in the VAS score of pelvic pain before and after treatment.
次要结局
未报告次要终点
研究者
研究点 (1)
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