跳至主要内容
临床试验/KCT0001972
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

发起方
Hallym University Medical Center-Kangnam

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