Objective evaluation of pain
Conditions
Interventions
Intervention type:
Name of intervention:
Dose form / Japanese Medical Device Nomenclature:
Route of administration / Site of application:
Dose per administration:
Dosing frequency / Frequency of use:
Sponsors
PaMeLa, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Age: patients between 20 and under 80 at the time of acquiring consent 2.Gender: males and females 3.Patients scheduled to undergo local anesthesia 4.One who has no abnormality or no abnormality in the brain 5.Patients who have consented to participate in this study with free will 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 |
|---|---|
| Digitized values of pain based on electroencephalogram | — |
Secondary
| Measure | Time frame |
|---|---|
| BIS value, NRS, SFMPQ-2 value | — |
Countries
Japan
Contacts
Public ContactKunihiro Nakai
University of Fukui Hospital
Outcome results
None listed