Clinical Trials Directory

Trials / Completed

CompletedNCT01919203

the Effective Bolus Dose of Remifentanil for Laryngeal Mask Airway (LMA) Insertion in Children

the Effective Bolus Dose of Remifentanil for Laryngeal Mask Airway (LMA) Insertion in Pediatric Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Sangjin Park · Academic / Other
Sex
All
Age
3 Years – 12 Years
Healthy volunteers
Not accepted

Summary

This research attempts to find the optimum dose of remifentanil that can prevent the unnecessary responses such as coughing, gagging, and movement when LMA is inserted during sevoflurane induction in pediatric patients.

Detailed description

Anaesthesia is induced by inhalation with 3% sevoflurane. A predetermined bolus dose of remifentanil is injected over 30 seconds. The LMA is attempted 60 seconds after bolus administration. The starting dose of remifentanil is 0.5μg/kg and a step size is 0.05μg/kg. If LMA insertion is successful or failed in previous patient, an decrement or increment of 0.05μg/kg remifentanil is injected to next patient, respectively.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilThe starting dose of remifentanil is 0.5μg/kg and a step size is 0.05μg/kg. If LMA insertion is successful or failed in previous patient, an decrement or increment of 0.05μg/kg remifentanil is injected to next patient, respectively.

Timeline

Start date
2013-08-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2013-08-08
Last updated
2015-07-16

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01919203. Inclusion in this directory is not an endorsement.