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
| Type | Name | Description |
|---|---|---|
| DRUG | dexmedetomidine | The 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). |
| DRUG | propofol | Propofol 2.0 mg/kg was administrated |
| DEVICE | laryngeal 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.