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WeightBS-BTNCT01763775

Clinical Trial of Transtek Body Fat Analyzer (GBF-1251-B & Other 3 Models)

A study testing Transtek 125X and Transtek 950D in people with Weight and Body Fat Disorder, run by Leo Wang at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Weight, Body Fat Disorder, Bone Mass
What is being tested?
Transtek 125X and Transtek 950D
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteChina
Study dates
Oct 2012to Oct 2012
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • male,female

Who cannot join

  • below 18 years old

Trial locations and contacts

1 site in 1 country.

China1 site
  • Wuhou District Hospital

    Chengdu, Sichuan, 610041

Other trials in China

About this study

Official title: Verify the Functions and Efficiency of Transtek (Trade Mark) Body Fat Analyzer, GBF-1251-B, BF-1255-B, BF-1256-B, and GBF-1257-B

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.
Read the detailed 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:
  4. Record the name, age, gender, and height of each subject.
  5. Let subject seated calmly for two minutes before test, dry the feet.
  6. Use device to measure weight, body fat, total body water, bone mass, and muscle mass; record reading value.
  7. For each subject, repeat 3) to get 3 pairs measurements.
  8. 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).
  9. Repeat step 1) to 5) for each subject.
  10. Note:
  11. No motion and speaking are allowed during the measurement.
  12. All DUT use the same algorithms and contact the patient at the same body locations (feet), and operate on the same frequency.
  13. Test environment: Temperature: 22±1℃; Relative humidity: 40~70%.
Being tested
Transtek 125X, Transtek 950D
Keywords
weight, total body water, body fat, muscle mass, bone mass
Medical subject headings
Body Weight

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Transtek 125XDevice

    Measuring weight, total body water, body fat, muscle mass, and bone mass. Measure each participants by Transtek 125X (GBF-1251-B, BF-1255-B, BF-1256-B, GBF-1257-B).

  • Transtek 950DDevice

    Measuring weight, total body water, body fat, muscle mass, and bone mass. Measure each participants by Transtek 950D (GBF-950-D).

Study groups in NCT01763775
Study groupRoleWhat they receive
Transtek 125XExperimentalWhich measured by DUT (Transtek 125X): GBF-1251-B, BF-1255-B, BF-1256-B, GBF-1257-B.
Receives: Device: Transtek 125X; Device: Transtek 950D
Transtek 950DExperimentalMeasured by Reference (Transtek 950D): GBF-950-D.
Receives: Device: Transtek 125X; Device: Transtek 950D

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. BMI (Body Mass Index)

    Body Fat, Total Body Water, Muscle Mass, Bone Mass

    Measured: 5 Day

Secondary outcomes (1)
  1. Weight

    Body Weight

    Measured: 5 Days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jan 2013 (estimated)
  2. Study startOct 2012
  3. Primary completionOct 2012
  4. Study completionOct 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Non-randomised
Intervention model
Factorial
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01763775
Sponsor's protocol ID
13001_Body Scale
Other IDs
BTS13001
Acronym
BS-BT
Status last verified
Jan 2013
First submitted
5 Jan 2013
Last updated
9 Jan 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Transtek 125X and Transtek 950D in people with Weight and Body Fat Disorder, run by Leo Wang at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Jan 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

BMI (Body Mass Index) (time frame: 5 Day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2013.

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