Healthy volunteer, Traumatic brain injury (TBI)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: I. Patients 20 y.o.<=Age<=65 y.o. patients suffering from TBI whose mechanism of injury was specified. II.Healthy volunteers 20 y.o.<=Age<=65 y.o., normal subjects
Exclusion criteria
Exclusion criteria: I. Patients 1. Subjects without ability to make informed consent 2. Subjects with any psychiatric disorder not due to TBI 3. Subjects with any organic brain disorder not due to TBI 4. Subjects with severe physical complication 5. Subjects with severe claustrophobia 6. Pregnant women 7. Subjects with tattoo 8. Subjects with metallic medical device in the body 9. Subjects who was considered to be inappropriate to participate in the study II. Healthy volunteers 1. Subjects without ability to make informed consent 2. Subjects with any psychiatric disorder 3. Subjects with any organic brain disorder 4. Subjects with severe physical complication 5. Subjects with severe claustrophobia 6. Subjects who has participated in other study in recent 6 months. 7. Pregnant women 8. Subjects with tattoo 9. Subjects with metallic medical device in the body 10. Subjects who was considered to be inappropriate to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Distribution volume and binding potential measured by positron emission tomography with [11C]PBB3 | — |
Secondary
| Measure | Time frame |
|---|---|
| Difference of spatial distribution of [11C]PBB3 and [11C]PIB Correlations between tau deposition and various clinical scales | — |
Countries
Japan
Contacts
National Institute of Radiological Sciences Molecular Imaging Center