跳至主要内容
临床试验/KCT0009376
KCT0009376尚未招募Unknown

Reliability and reproducibility evaluation study of portable body composition analyzer (Fitrus Light)

Cheonan Korean Medicine Hospital of Daejeon University0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
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

入排标准

年龄范围
19(Year) 至 64(Year)(—)
性别
All

入选标准

  • (1) Adults between the ages of 19 and 64 years old
  • (2) who have given voluntary written consent to participate in this clinical study

排除标准

  • (1) Have taken dietary supplements or medications for weight control within 4 weeks of the first visit
  • (2) Uncontrolled psychiatric illness, alcoholics
  • (3) Participated in another clinical study within 1 month of the screening visit and received an intervention
  • (4) Pregnant or breastfeeding women
  • (5) Have had an implantable medical device, such as a pacemaker, etc.
  • (6) Have had metallic materials inserted into the body
  • (7) Those who have mobility problems and are unable to position themselves correctly for the examination.
  • (8) Those with contagious diseases or wounds on the palms or soles of the feet
  • (9) Those deemed inappropriate by the researcher to participate in the study

研究者

发起方
Cheonan Korean Medicine Hospital of Daejeon University

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