Clinical Trials Directory

Trials / Completed

CompletedNCT04563260

Effect of Palonosetron on Remifentanil for Preventing Emergence Cough in Female

Effect of Palonosetron on Effect-site Concentration of Remifentanil for Preventing Emergence Cough During General Anesthesia in Female Patients Undergoing Laparoscopic Cholecystectomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
Female
Age
19 Years – 85 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 female patients who receive the palonosetron or not.

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
DRUGNormal saline injectionNormal saline 2 mL, intravenous injection
DRUGPalonosetron Injection [Aloxi]Palonosetron 1.5 mL (0.075 mg) + Normal saline 0.5 mL, intravenous injection

Timeline

Start date
2020-10-07
Primary completion
2021-03-19
Completion
2021-03-19
First posted
2020-09-24
Last updated
2021-05-11

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04563260. Inclusion in this directory is not an endorsement.