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Dosing Study of Remifentanil for Smooth Removal of the Laryngeal Mask Airway (LMA)

Drug Usage Clinical Trial

Official title:
Effect-site Concentration of Remifentanil for Smooth Removal of the LMA From Propofol Anesthesia

Clinical Trial Summary

The investigators attempted to determine the optimal effect-site concentration of remifentanil for smooth removal of the LMA from propofol anesthesia.

Clinical Trial Description

At the end of the surgery, propofol infusion was stopped and remifentanil was titrated to predetermined (initial concentration 1.0 ng/ml for the first patient). LMA removal was performed when the patients opened their eyes and spontaneous respiration and adequate tidal volume and ventilatory frequency were confirmed. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01931683
Study type Interventional
Source Ajou University School of Medicine
Contact
Status Completed
Phase Phase 4
Start date October 2013
Completion date February 2014
View Details
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