Healthy volunteers
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Healthy volunteers. 2)Subjects who signed, based on his/her free will, to the clinical trial agreement with full understanding of the purpose of this conducted trial and its insights.
Exclusion criteria
Exclusion criteria: 1)Subjects who have donated 200 mL blood within 1 month, or 400 mL blood within 3 month. 2)Subjects who have taken aspirin or drugs with antiplatelet effect within 1 week. 3)Subjects with hypertension or hypotension. 4)Subjects with poor condition on a blood collecting day. 5)Subjects whom the doctor considered to be unsuitable for this study. 6)Subjects who are unable to put restrictions on diets (ex. foods and drinks are prohibited within 4 hours prior to blood collection, high fat meals should be avoided since 1 day before blood collection).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Platelet aggregation activity(Platelet Aggregation Threshold Index:PATI) | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum thromboxane B2 concentration | — |
Countries
Japan
Contacts
Tokyo University of Science Faculty of Pharmaceutical Sciences