Clinical Trials Directory

Trials / Completed

CompletedNCT01852539

Dexmedetomidine for Laryngeal Mask Airway Insertion

Optimal Dose of Dexmedetomidine for Laryngeal Mask Airway Insertion During Propofol Induction

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

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGdexmedetomidineThe dose of dexmedetomidine was determined by modified Dixon's up-and-down method, starting from 0.5 μg/kg (0.1 μg/kg as a step size).
DRUGpropofolPropofol 2.0 mg/kg was administrated
DEVICElaryngeal mask airway (LMA)The insertion of laryngeal mask airway (LMA) was attempted, after confirming the loss of eyelash reflex,the bispectral index (BIS) score decreased below 60.

Timeline

Start date
2013-07-01
Primary completion
2013-08-01
Completion
2013-08-01
First posted
2013-05-13
Last updated
2014-04-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01852539. Inclusion in this directory is not an endorsement.