The study to reduce the complications associated with BIS electrodes
Not Applicable
- Conditions
- Patients, who are scheduled for elective surgery under general anesthesia with BIS monitoring.
- Registration Number
- JPRN-UMIN000023717
- Lead Sponsor
- Department of Anesthesiology and Resuscitology, Shinshu University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are scheduled for surgery in prone position or with cardiopulmonary bypass are excluded. Patients with dermatosis, allergy or mental disorder are excluded. Patients who received chemotherapy, radiotherapy, corticosteroid, nonsteroidal anti-inflammatory drugs, opioids or psychotropic agents are excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The incidence of skin lesion associated with BIS electrodes
- Secondary Outcome Measures
Name Time Method Patient's pain when BIS electrodes are applied