Assessment of Phase Lag Entropy(PLE) monitor for the sedation levels using propofol
Not Applicable
Recruiting
- Conditions
- Diseases of the musculo-skeletal system and connective tissue
- Registration Number
- KCT0002542
- Lead Sponsor
- Soon Chun Hyang University Hospital Seoul
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
adult patients ( >18 yr old) who undergoing upper arm surgery under brachial plexus block using ultrasonogram
Healthy patient who is American Society of Anesthesiology (ASA) physical status 1or 2.
Exclusion Criteria
-patient who has CNS disease, past history of CNS disease, and neurological disorder
- patient who has been taken anticonvulsant agent, sedatives, analgesics, and hypnotics .
- significant hepatic disease or renal disease
- obesity (BMI>30)
_ Obstructive sleep apnea
- hypersensitivity to propofol or local anesthetics
- hypersensitivity to bean or peanut
_ pregnant woman
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method correlation of OAA/S Scale and PLE
- Secondary Outcome Measures
Name Time Method comparison PLE with BIS