Physician-led clinical trial for the development of PMS-2, a device to objectively monitor the efficacy of analgesic drugs for postoperative pai
- Conditions
- Patients scheduled to undergo surgery under general anesthesiageneral 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
(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
(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
Name Time Method
- Secondary Outcome Measures
Name Time Method