Clinical Trials Directory

Trials / Completed

CompletedNCT04407078

Sugammadex on Remifentanil Ce for Preventing Emergence Cough in Female

Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
Female
Age
19 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the optimal Ce of remifentanil for preventing emergence cough following extubation during general anesthesia in female who are reversed with sugammadex or neostigmine.

Detailed description

Remifentanil is a potent ultrashort-acting opioid, with rapid onset and offset of drug effect. It allows rapid anesthetic emergence even after a prolonged infusion, and decreases the at-risk time during extubation. In addition, cough suppression of remifentanil enables smooth extubation with reduced complications. However, the infusion of remifentanil suppresses the emergence cough effectively in clinical practice, whereas it still delays the awakening from anesthesia, resulting in prolonged emergence time. Reduced Ce of remifentanil during emergence would decrease the adverse events that are associated with remifentanil infusion.

Conditions

Interventions

TypeNameDescription
DRUGSugammadex Injectable ProductSugammadex of 2 mg/kg is injected.
DRUGNeostigmine Injectable ProductNeostigmine of 50 ug/kg and Glycopyrrolate of 10 ug/kg are injected.

Timeline

Start date
2019-12-02
Primary completion
2021-01-06
Completion
2021-01-06
First posted
2020-05-29
Last updated
2021-01-08

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04407078. Inclusion in this directory is not an endorsement.