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Physician-led clinical trial for the development of PMS-2, a device to objectively monitor the efficacy of analgesic drugs for postoperative pai

Not Applicable
Recruiting
Conditions
Patients scheduled to undergo surgery under general anesthesia
general anesthesia
Registration Number
JPRN-jRCT1052230029
Lead Sponsor
akai Kunihiro
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

(1) Patients who are 20 years of age or older at the time consent is obtained
(2) Patients scheduled to undergo surgery under general anesthesia
(3) Gender: any gender
(4) Patients who have given written consent of their own free will

Exclusion Criteria

(1) Patients with known or pre-existing neurological disorders such as epilepsy
(2) Patients taking narcotic analgesics
(3) Patients with a history of cerebral infarction or hemorrhage
(4) Patients with a history of other organic brain diseases
(5) Patients already diagnosed with chronic pain
(6) Patients with cardiac pacemakers or electronic implants
(7) Patients with severe visual impairment
(8) Women of childbearing potential
(9) Patients with apparent cognitive impairment
(10) Patients scheduled for an MRI scan at the time of EEG electrode placement during the observation period
(11) Patients who are judged by the investigator or subinvestigator to be inappropriate to participate in this clinical trial.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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