Influence of gender on the effect-site concentration of remifentanil for the the conventional laryngeal mask airway insertion during target-controlled infusion of propofol
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0000151
- Lead Sponsor
- Hallym University Medical Center-Kangnam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
After obtaining the approval of institutional ethics committe and written informed consent, patients aged 18-60 yr of ASA physical status I or II scheduled to undergo elective monior surgery requiring general anesthesia.
Exclusion Criteria
Patients with a potentially difficult airway (Mallampati classification III or IV. Cervical spine disease, or a mouth opening of < 2.5 cm), signs of upper respiratory infection, history of reactive airway disease or gastro-esophageal reflux, and a history of allergic reaction to the anesthesia drugs (propofol).
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method EC50 and EC95 of remifentanil for successful LMA insertion for men and women
- Secondary Outcome Measures
Name Time Method