Clinical Trials Directory

Trials / Completed

CompletedNCT02382354

Remifentanil for the I-gel and Laryngeal Mask Airway Insertion

Comparison of the Effect-site Concentration of Remifentanil for Insertion of the I-gel and Laryngeal Mask Airway During Propofol Anesthesia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
Female
Age
19 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Structural differences of supraglottic airway devices could influence the different compressive forces in the oropharyngeal cavities, and require different depth of anesthesia. The addition of remifentanil during propofol anesthesia facilitates the insertion of laryngeal mask airway (LMA) with minimal adverse hemodynamic disturbances. This study was designed to determine the effect-site concentration of remifentanil in 50% of patients (EC50) and 95% of patients (EC95) for successful i- gel insertion, and compare those for LMA insertion during propofol target-controlled infusion (TCI).

Detailed description

Anesthesia was induced with propofol TCI at the effect-site concentration of 5 μg/ml, and the predetermined effect-site concentration of remifentanil was started simultaneously. The remifentanil concentration was determined using modified Dixon's up-and-down method (initial concentration: 3.0 ng/ml, step size: 0.5 ng/ml). Five minutes later, i- gel or LMA insertion was attempted. The response of the patients to the insertion of LMA was classified as either 'movement' or 'no movement'.

Conditions

Interventions

TypeNameDescription
DRUGremifentanilThe predetermined effect-site concentration of remifentanil was started using modified Dixon's up-and-down method
DEVICEi-gelI-gel insertion was inserted 5 min after anesthesia induction
DEVICElaryngeal mask airwaylaryngeal mask airway insertion was inserted 5 min after anesthesia induction
DRUGpropofolAnesthesia was induced with propofol target-controlled infusion at the effect-site concentration of 5 μg/ml

Timeline

Start date
2015-03-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2015-03-06
Last updated
2015-10-14

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02382354. Inclusion in this directory is not an endorsement.