Healthy adult
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Subjects who are judged as healthy by self-reported health questionnaire 2. Subjects who agree to participate in this study with a written informed consent after receiving sufficient explanation relating to this study
Exclusion criteria
Exclusion criteria: 1. Subjects who have respiratory, gastrointestinal, hepatic/gallbladder/pancreatic, hematologic, renal, endocrine, cardiovascular and/or mental disease 2. Subjects who had a serious injury or surgical history within 12 weeks prior to this study 3. Pre- or post-menopausal women having obvious changes in physical condition 4. Subjects donate either 400ml or 200ml whole blood or blood component within four weeks prior to this study 5. Subjects who are pregnant or lactating, or subjects who expect to be pregnant during this study 6. Subjects who have cognitive disorder or who have possibility of the disorder 7. Subjects who participated and took the study drug in other clinical trials within four weeks prior to this study 8. Subjects who are judges as unsuitable for this study by the principal investigator or subinvestigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurability in blood samples | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Correlation between electrical conductivity (viscosity) of whole blood and plasma 2. Correlation between electrical conductivity (viscosity) of whole blood or plasma and whole blood viscosity 3. Correlation between electrical conductivity (viscosity) of whole blood or plasma and blood test values such as glycolipid levels 4. Correlation between electrical conductivity (viscosity) of whole blood or plasma and AGEs score 5. Correlation between electrical conductivity (viscosity) of whole blood or plasma and body measurements 6. Adverse events | — |
Countries
Japan
Contacts
University of Miyazaki Health-Care Research Department, University of Miyazaki