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Clinical Trials/KCT0009376
KCT0009376
Not yet recruiting
未知

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

Cheonan Korean Medicine Hospital of Daejeon University0 sites50 target enrollmentTBD
ConditionsNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Not Applicable
Sponsor
Cheonan Korean Medicine Hospital of Daejeon University
Enrollment
50
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Cheonan Korean Medicine Hospital of Daejeon University

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • (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

Outcomes

Primary Outcomes

Not specified

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