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Dosing Study of Remifentanil for Smooth Removal of the Laryngeal Mask Airway (LMA)

Effect-site Concentration of Remifentanil for Smooth Removal of the LMA From Propofol Anesthesia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01931683
Enrollment
27
Registered
2013-08-29
Start date
2013-10-31
Completion date
2014-02-28
Last updated
2014-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Drug Usage

Keywords

LMA removal, remifentanil, propofol

Brief summary

The investigators attempted to determine the optimal effect-site concentration of remifentanil for smooth removal of the LMA from propofol anesthesia.

Detailed description

At the end of the surgery, propofol infusion was stopped and remifentanil was titrated to predetermined (initial concentration 1.0 ng/ml for the first patient). LMA removal was performed when the patients opened their eyes and spontaneous respiration and adequate tidal volume and ventilatory frequency were confirmed.

Interventions

DRUGremifentanil

The concentration of remifentanil was determined by modified Dixon's up-and-down method, starting from 1.0 ng/ml (0.2 ng/ml as a step size)

LMA was removed when the patients opened their eyes, and spontaneous respiration and adequate tidal volume and ventilatory frequency were confirmed

Sponsors

Ajou University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
smooth removal of LMAfrom end of surgery to removal of LMA (participants will be followed for the emergence periods, an expected average of 15 min).the response of patients to the removal of LMA (classified as either 'success \[smooth emergence\]' or 'failure') during infusion of remifentanil.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026