Nothing in particular
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers who gave consent to participate in the research, on the premise that no coercive force was applied to their research cooperation
Exclusion criteria
Exclusion criteria: Inappropriate blood collection specimens (specimen coagulation) Volunteers administered medications affecting APTT measurement Volunteers at risk for side effects such as bleeding tendency Volunteers with APTT outside the reference range at the initial blood draw
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| APTT | — |
Contacts
Juntendo University Urayasu Hospital