Cerebrovascular disease
Conditions
Interventions
Attach the sensor of the near infrared light monitor to the forehead part and the sensor for indocyanine green to the auricle part.Continuous administration of 0.5-2.0 mg of indocyanine green from the
Sponsors
Kansai Rosai Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Person who receives examination or treatment because of cerebrovascular disease.
Exclusion criteria
Exclusion criteria: Person who has a history of indocyanin green allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To nvestigate whether the near infrared monitor can capture the apparent oxygen saturation change induced by indocyanine green administered from the cerebral artery | — |
Secondary
| Measure | Time frame |
|---|---|
| To investigate what factors infulence the near-infrared monitor. | — |
Countries
Japan
Contacts
Public ContactHiroshi Ueyama
Kansai Rosai Hospital Department of Anesthesiology
Outcome results
None listed