Clinical Trials Directory

Trials / Completed

CompletedNCT03583021

Sugammadex on Remifentanil Ce for Preventing Emergence Cough in Male

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
Male
Age
65 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this study is to investigate the optimal Ce of remifentanil for preventing emergence cough following extubation during general anesthesia in male patients 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 3 mg/kg is injected.
DRUGNeostigmine Injectable ProductNeostigmine of 50 ug/kg and Glycopyrrolate of 10 ug/kg are injected.

Timeline

Start date
2018-06-25
Primary completion
2018-10-31
Completion
2018-12-31
First posted
2018-07-11
Last updated
2020-05-29

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03583021. Inclusion in this directory is not an endorsement.

Sugammadex on Remifentanil Ce for Preventing Emergence Cough in Male (NCT03583021) · Clinical Trials Directory