A comparison of effect of dexmedetomidine according to body compositio
Not Applicable
- Conditions
- Not Applicable
- Registration Number
- KCT0005737
- Lead Sponsor
- Jeonbuk National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 280
Inclusion Criteria
• 18-75 years, ASA/PS I or II, patients who were scheduled to undergo upper of lower extremity surgery under regional anesthesia
• patients with informed consent
Exclusion Criteria
1. patient refusal
2. severe hepatorenal impairment
3. difficulty of communication such as hearing impairment
4. metal implant due to previous surgery
5. cardiac pacemaker of ICD
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Required dose of dexmedotomidine for LOC µg)
- Secondary Outcome Measures
Name Time Method time to LOC, sedation level at LOC, BIS at LOC, time to BIS 80 and 90, vital signs