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sefulness of neuromuscular blocker in elderly patients

Not Applicable
Completed
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
Inclusion Criteria

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).

Exclusion Criteria

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
NameTimeMethod
success rate on first attempt of i-gel insertion
Secondary Outcome Measures
NameTimeMethod
device insertion time for succeful ventilation
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