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Dexmedetomidine for Laryngeal Mask Airway Insertion

A

Ajou University School of Medicine

Status and phase

Completed
Phase 4

Conditions

Drug Usage

Treatments

Drug: propofol
Device: laryngeal mask airway (LMA)
Drug: dexmedetomidine

Study type

Interventional

Funder types

Other

Identifiers

NCT01852539
AJIRB-MED-CT4-13-045

Details and patient eligibility

About

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.

Full 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.

Enrollment

22 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-II patients undergoing general anesthesia for short elective surgery (<1 hr)

Exclusion criteria

  • G-E reflux
  • obesity (BMI>30)
  • anticipated difficult airway

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

Double Blind

22 participants in 1 patient group

dexmedetomidine
Experimental group
Description:
After intravenous infusion of dexmedetomidine for 2 min, propofol 2.0 mg/kg was administrated. And laryngeal mask airway device was inserted(LMA # 3,4).
Treatment:
Drug: dexmedetomidine
Device: laryngeal mask airway (LMA)
Drug: propofol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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