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Performance evaluation of noninvasive lipid measurement device by fat load test

Performance evaluation of noninvasive lipid measurement device by fat load test - Performance evaluation of noninvasive lipid measurement device by fat load test

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027559
Enrollment
24
Registered
2017-05-31
Start date
2017-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Test with fat load

Sponsors

Hokkaido Information University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.subjects whose TG is 50 mg / dl or more and less than 150 mg / dl, or 150 mg / dl or more.

Exclusion criteria

Exclusion criteria: 1.Subjects using anticoagulants (such as warfarin), antiplatelet drugs (aspirin, clopidogrel, ticlopidine, cilostazol etc.), coagulation accelerators (calcium solution, thrombin, vitamin K, etc.). 2.Subjects with blood clotting disease (hemophilia, platelet asthenia, warfarin administration, liver failure, etc). 3.Subjects who may have allergic symptoms in dairy products. 4.Subjects who received physician treatment, medication, and life guiduance for obesity, dyslipidemia, diabetes. 5.Subjects suffering from severe cerebrovascular disease, heart disease, liver disease, kidney disease, gastrointestinal disease, endocrine metabolic disease, infection requiring notification. 6.Subjects using pacemakers and defibrillators. 7.Subjects who have injuries, atopic skin diseases, contact dermatitis, rashes, etc. on the skin of the upper arm. 8.Subjects with major surgical history relevant to the digestive system. 9.Subjects with unusually high, low blood pressure, abnormal hematological data, severe anemia. 10.Pre- or post-menopausal women complaining of obvious physical changes. 11.Excess smokers and regulars alcohol addicts or subjects with eating disordered lifestyle. 12.Subjects who donated a predetermined amount of blood in a given period. 13.Pregnant or lactating women or women who expect to be pregnant during this study. 14.Subjects who currently participate in other clinical trials, or participated within the last 4 weeks prior to the current study. 15.Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Blood triglyceride level by noninvasive measuring instrument Blood triglyceride concentration by free glycerol elimination method

Secondary

MeasureTime frame
Height, body weight, BMI, body fat percentage, blood pressure, pulse rate, blood flow, skin surface temperature,Ht,TC, LDL-C, HDL-C,casual blood glucose level,Apolipoprotein,Lipoprotein fraction,AST, ALT, r-GTP, ALP, LDH,BUN, CRE, UA, Alb, TP, T-Bil, CPK

Countries

Japan

Contacts

Public ContactDir. Prof. Jun NISHIHIRA, M.D., Ph.D.

Hokkaido Information University Health Information Science Center

nishihira@do-johodai.ac.jp011-385-4430

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026