Patient who is scheduled for surgery, or hospitalization
Conditions
Interventions
Intervention type:DEVICE
Name of intervention:Biological information monitoring
Dose form / Japanese Medical Device Nomenclature:DEVICE
Electroencephalograph, Device for quantitative analysis of pain
Sponsors
PaMeLa, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age:patients over 20 at the time of acquiring consent 2. Gender:male and female 3. Patients who are scheduled for surgery, or hospitalization 4. One who currently has no abnormality or have had no abnormality of brain in the past 5. Patients who have consented to participate in this study after receiving sufficient explanation for this study and gained sufficient understandings
Exclusion criteria
Exclusion criteria: 1. A person who is taking medication for mental illness 2. A person who is already diagnosed with chronic pain 3. A patient who was judged as inappropriate as a research subject by the research director
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Digitalized pain value based on electroencephalogram Numerical pain value from PainVision | — |
Secondary
| Measure | Time frame |
|---|---|
| BIS value, NRS, SFMPQ-2 value, Pulse Wave Amplitude, Skin Conductance Response, Pulse rate | — |
Countries
Japan
Contacts
Public ContactKunihiro Nakai
University of Fukui Hospital
Outcome results
None listed