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临床试验/JPRN-UMIN000027559
JPRN-UMIN000027559已完成未知

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

Hokkaido Information University0 个研究点目标入组 24 人开始时间: 2017年5月31日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 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.

研究者

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