Clinical Trials Directory

Trials / Completed

CompletedNCT02973724

EC95 of Remifentanil for Preventing Cough

Predicted EC95 of Effect-site Concentration of Remifentanil for Preventing Cough After Laryngomicrosurgery From Propofol Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The investigator designed this study to investigate remifentanil effect-site concentration in 95% of patients (EC95) for preventing cough after laryngomicrosurgery 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). Extubation was performed when the patients opened their eyes and spontaneous respiration and adequate tidal volume and ventilatory frequency were confirmed.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilThe concentration of remifentanil was determined by biased-coin up and down design, starting from 1.0 ng/ml (0.4 ng/ml as a step size)
DRUGPropofol anesthesiaAnesthesia was induced with propofol target-controlled infusion at an effect-site concentration of 5.0 μg/ml.

Timeline

Start date
2016-11-01
Primary completion
2017-06-01
Completion
2017-06-01
First posted
2016-11-25
Last updated
2017-06-09

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02973724. Inclusion in this directory is not an endorsement.