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Clinical Trial Summary

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. Device Under Test (DUT): Transtek Body Fat Analyzer, Model: GBF-1251-B, BF-1255-B, BF-1256-B, and GBF-1257-B.

4. Comparison device: Transtek, Glass Body Fat Analyzer, GBF-950-D.

5. Study endpoints: DUT and the comparison device are substantial equivalence.

6. Statistical methodology used: Description of statistical methods.


Clinical Trial Description

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.

2. Target Subject:

The subject database shall contain at least 25 male and 25 female subjects and all above 18 years old.

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-1251-B, BF-1255-B, BF-1256-B, and GBF-1257-B; and reference device: GBF-950-D).

6. Repeat step 1) to 5) for each subject.

4. Note:

1. No motion and speaking are allowed during the measurement.

2. All DUT use the same algorithms and contact the patient at the same body locations (feet), and operate on the same frequency.

3. Test environment: Temperature: 22±1℃; Relative humidity: 40~70%. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01763775
Study type Interventional
Source BTS International
Contact
Status Completed
Phase N/A
Start date October 2012
Completion date October 2012

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