Body Fat Disorder Clinical Trial
Official title:
Verify the Functions and Efficiency of Transtek Glass Body Analyzer, GBF-830, GBF-835, GBF-950, SA-15
The clinical protocol of the clinical testing of this device:
1. Objective of the test: To verify the functions and efficiency of devices.
2. Test methods and procedures: Comparison Test.
3. DUT: Transtek Glass Body Analyzer, Model: GBF-830, GBF-835, GBF-950, and SA-15.
4. Comparison device: Scaleman Body Fat Scales, FS-148BW1 (Predicate Device).
5. Study endpoints: Transtek devices and the predicate device are substantial equivalence.
6. Statistical methodology used: Description of statistical methods.
7. Result: Efficiencies of Transtek devices and predicate device are in the same level.
Hospital Information The data was collected by West China Medical College Clinical
Investigator Team at Wuhou District Hospital, No. 9 Tongzilin Road, Wuhou District, Chengdu
610041, P. R. China.
Investigator: Catharine Zhang, Nurse A; Vivian Luo, Nurse B; Dr. James Zhu, Sponsor.
Contact Dr. James Zhu Tel: +86 1330 8036568 Used Equipments DUT (Device Under Test):
Transtek Glass Body Analyzer, GBF-830, GBF-835, GBF-950, and SA-15.
Reference Device: Scaleman Body Fat Scales, FS-148BW1 (Predicate Device). Test Protocol
1. Test Purpose:
The aim of clinical test is to collect weight, body fat, total body water, bone mass,
and muscle mass reading value which measured by DUT and reference device.
Note: GBF-835 has not total body water, bone mass, and muscle mass functions. So it
just collects weight and body fat data.
2. Target Subject:
The subject database shall contain at least 25 male and 25 female subjects and all
above 18 years old. Patient's population analysis is bellow.
3. Test procedures 1) Record the name, age, gender, and height of each subject. 2) Let
subject seated calmly for two minutes before test, dry the feet. 3) Use device to
measure weight, body fat, total body water, bone mass, and muscle mass; record reading
value.
4) For each subject, repeat 3) to get 3 pairs measurements. 5) Repeat step 1) to 4) for
every device (DUT: GBF-830, GBF-835, GBF-950, and SA-15; and reference device: FS-148BW1).
6) Repeat step 1) to 5) for each subject. 5. Note:
1. No motion and speaking are allowed during the measurement.
2. All DUT use the same algorithms, have the same number of electrodes and contact the
patient at the same body locations (feet), and operate on the same frequency.
3. Test environment: Temperature: 20±1℃; Relative humidity: 40~50%.
;
Observational Model: Cohort, Time Perspective: Retrospective
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