KCT0001972已完成未知
A one-group clinical study for evaluation of efficacy and safety by YESLEG as a non-operative treatment in bowleg patients
Hallym University Medical Center-Kangnam0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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 50(Year)(—)
- 性别
- Female
入选标准
- •1. Female patient whose age is between 18 and 50, who is not pregnant nor planning for pregnancy in 3 months.
- •2. Female patient who has O-shaped bow leg whose leg gap is over 5cm, or X-shaped bow leg whose distance between both feet is over 3cm
- •3. Female patient who takes pain-relief medications at least one time in menstruation period due to pain.
- •4. Female patient who is not on a diet in research period.
- •5. Patient who can write written consent and keep on rules regarding the clinical trial.
排除标准
- •1. Patient who has cardiovascular disease or takes anticoagulants.
- •2. Patient who takes drugs regulary for any underlying diseases.
- •3. Patient who has dermatologic diseases.
- •4. Patient who has hematologic neoplasm.
- •5. Patient who is pregnant or planning for pregnancy in 6 months.
- •6. Patient who is getting other treatments due to low back pain.
- •7. Patient who had musculoskeletal surgery such as correction of genu varum or artificial hip joint replacement
- •8. Patient who was enrolled in other clinical trials in 4 weeks.
- •9. Patient who is inadequate for cilinical trial by researchers' opinion.
研究者
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