Examination of the sensory threshold in patients using perioperative opioid.
Not Applicable
- Conditions
- none
- Registration Number
- JPRN-UMIN000030713
- Lead Sponsor
- Kitasato University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1.Dementia, consciousness disorder, and psychiatric disorder. 2.Aphasia, auditory disorder, and total blind. 3.Sensory disturbance. 4.Patients who can not equip an electrode because of the skin lesions. 5.Patients who use an implanted pacemaker, and a spinal cord stimulation. 6.Patients who use an implanted defibrillator. 7.Patients who use an opioid before surgery. 8.Patients who use a regional anesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method