Comparison effects of induction and recovery profile from sevoflurane anesthesia in normal and cognitive dysfunction elderly patients
Not Applicable
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Registration Number
- KCT0003884
- Lead Sponsor
- Inje University Haeundae Paik Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Elderly patients over 65 years of age who undergo orthopedic surgery under general anesthesia
Exclusion Criteria
Patients and caregivers do not want to participate this study.
American Society of Anesthesiologists classification ? or more
Patients with a BMI greater than 30
A history of neuromuscular deficit or major psychiatric disorder
Drug or alcohol abuse
Poorly controlled hypertension,
Presence of chronic obstructive pulmonary disease
Heart or renal failure
Chronic opioid or sedative use
Hypersensitivity to sevoflurane anesthetics
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method End-tidal sevoflurane concentration
- Secondary Outcome Measures
Name Time Method Modified Observer's Alertness/Sedation scale (MOAA/S)