Healthy volunteers
Conditions
Interventions
None listed
Sponsors
Faculty of Medicine, Kyushu university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Age:>=20 and <=60 years old at obtaining informed consent 2)Body fat percentage:>=20% for male, and >= 30% for female 3)Normal hematopoietic function 4)Suitable as a subject as results of screening test conducted after obtaining informed consent 5)Participate this trial based on subject's own free will and give informed consent in written form
Exclusion criteria
Exclusion criteria: 1)Active or medical history of infectious disease within 3 months before registration 2)Past or present critical dysfunction of digestive organ, cardiovascular system, kidney, liver, or blood coagulation system 3)Positive for HBs antigen, HCV antibody, or HIV antibody 4)Blood sampling within 1 month or blood component sampling within 2 weeks before registration 5)Dosing anticoagulant agent 6)APTT >= 48 sec or PT >= 15sec 7)Cancer required treatment 8)Congenital or metabolic bone disease 9)Medical history of drug dependency or alcoholism 10)Participate other clinical research within 3 months before this trial 11)Medical history of drug hypersensitivity 12)Pregnant, capable of pregnancy and lactating women 13)Unsuitable for this trial judged by PI or SI
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility of fabrication of stem cell plug derived from human tissue | — |
Countries
Japan
Outcome results
None listed