Effects of earmuffs and eye masks on propofol sedation during spinal anesthesia
Not Applicable
- Conditions
- IV sedation during spinal anesthesia for lower limb orthopedic surgery
- Registration Number
- JPRN-UMIN000043496
- Lead Sponsor
- Seoul National University Bundang Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
- General anesthesia - Combined spinal-epidural anesthesia - Patients who do not want sedation during operation - H/O allergic reaction to propofol - Lateral decubitus or prone position - Day surgery - Hearing impairment - Substance abuse - Cognitive or memory impairment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Propofol usage (mg/kg/hour)
- Secondary Outcome Measures
Name Time Method Propofol target concentration, the time to achieve proper sedation confirmed with the BIS score under 80, spinal block level, satisfaction score about sedation during anesthesia, PCA/antiemetics usage during 24 postoperative hours