Dexmedetomidine for Laryngeal Mask Airway Insertion

Status Completed

Clinical Trial Summary

The investigators attempted to determine the optimal dose of dexmedetomidine required for the successful insertion of LMA during propofol induction without a neuromuscular blocking agent.

Clinical Trial Description

After a predetermined bolus dose of dexmedetomidine was injected over 2 min, anesthesia was induced with propofol 2.0 mg/kg. After confirming the loss of eyelash reflex and the bispectral index (BIS) score decreased below 60, the insertion of LMA was attempted. ;

Study Design

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

Related Conditions & MeSH terms

Drug Usage

Clinical Trial Details

NCT number	NCT01852539
Study type	Interventional
Source	Ajou University School of Medicine
Contact
Status	Completed
Phase	Phase 4
Start date	July 2013
Completion date	August 2013

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