sefulness of neuromuscular blocker in elderly patients
- Conditions
- Not Applicable
- Registration Number
- KCT0003616
- Lead Sponsor
- Konyang University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 58
1) the patient who have decided to voluntarily participate in the study and have signed the informed consent.
2) 65 ~ 85 year old
3) patients undergoing elective surgery which is expected ending within 2 hours
4) American Society of Anesthesiologist Patient Status I~III(I is a normal healthy patient, II is patient with mild systemic disease and III is patient with moderate systemic disease).
1) the patient who refused to participate in this study
2) under 65 years old, 86 years old or order
3) emergency operation
4) obesity (Body mass index >35kg/m2)
5) pharyngeal pathology
6) risk of gastroespophageal reflux
7) respiratory disease
8) wobbling teet
9) psychiatric disease or cognitive disorder
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method success rate on first attempt of i-gel insertion
- Secondary Outcome Measures
Name Time Method device insertion time for succeful ventilation