Clinical Trials Directory

Trials / Completed

CompletedNCT01456299

Laryngeal Mask Airway (LMA) Insertion With Sevoflurane and Remifentanil

Target-controlled Infusion of Remifentanil for Laryngeal Mask Airway Insertion During Sevoflurane Induction in Adults

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
102 (actual)
Sponsor
Gachon University Gil Medical Center · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to determine the most suitable effect-site concentration of remifentanil for the LMA insertion during inhaled induction with 8% sevoflurane in adults.

Detailed description

For practical purposes, opioids with the ability to suppress upper airway reflexes have been used to facilitate insertion of the LMA during anaesthesia induction. To date, however, there have been no published reports addressing the use of remifentanil to facilitate LMA insertion during sevoflurane inhalation induction in adults. Therefore, the purpose of this study was to determine the most suitable effect-site concentration of remifentanil target-controlled infusion (TCI) for the LMA insertion during inhaled induction with 8% sevoflurane in adults.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanil 1"Remifentanil 1": "The R1 group, which received a target effect-site remifentanil concentration of 1 ng/ml.
DRUGControlThe control group, which received an infusion of normal saline
DRUGRemifentanil 2"Remifentanil 2": "The R2group, which received a target effect-site remifentanil concentration of 2 ng/ml.

Timeline

Start date
2011-04-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2011-10-20
Last updated
2019-03-15
Results posted
2014-04-04

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01456299. Inclusion in this directory is not an endorsement.