Clinical Trials Directory

Trials / Completed

CompletedNCT03173339

Influence of Remifentanil on Postoperative Sore Throat in Patients Undergoing General Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
92 (actual)
Sponsor
Keimyung University Dongsan Medical Center · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This investigation is planned to compare the incidence and severity of postoperative sore throat according to the dose of remifentanil.

Conditions

Interventions

TypeNameDescription
PROCEDUREEndotracheal intubation using laryngoscopeEndotracheal intubation was done using laryngoscope for general anesthesia.
DRUGHigh remifentanilRemifentanil was started as 0.25 mcg/kg/min. Remifentanil dose was adjusted to maintain blood pressure (20% of preoperative blood pressure) and bispectral index (40-60) by 0.05 mcg/kg/min.
DRUGLow remifentanilRemifentanil was administered as 0.1 mcg/kg/min.
DRUGHigh sevofluraneSevoflurane was started as 0.5 MAC. Sevoflurane dose was adjusted to maintain blood pressure (20% of preoperative blood pressure) and bispectral index (40-60) by 0.2 %.
DRUGLow sevofluraneSevoflurane was administered as 0.5 MAC.

Timeline

Start date
2017-06-01
Primary completion
2017-08-24
Completion
2017-08-24
First posted
2017-06-01
Last updated
2017-08-25

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03173339. Inclusion in this directory is not an endorsement.