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Trials / Completed

CompletedNCT02334046

Remifentanil for Smooth Emergence in Elderly Patients

Effect-site Concentration of Remifentanil for Preventing Cough During Emergence in Elderly Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
47 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Elderly patients show different pharmacokinetic and pharmacodynamic variables and usually need smaller doses of anaesthetic drugs than younger patients. The purpose of this study was to investigate the optimal effect-site concentration of remifentanil for preventing cough during emergence in elderly patients under sevoflurane and remifentanil anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilRemifentanil was maintained at predetermined effect-site concentration during the periextubation period (initial concentration: 1.8 ng/ml) in elderly patients (65-80 years) .
DRUGRemifentanilRemifentanil was maintained at predetermined effect-site concentration during the periextubation period (initial concentration: 1.8 ng/ml) in adult patients (20-60 years) .
DRUGSevofluraneAnesthesia was maintained with sevoflurane with 1.5-2.0 vol% in air/50%oxygen mixture, and sevoflurane was adjusted to about 1.0 vol% 10 min before end of surgery.

Timeline

Start date
2015-02-01
Primary completion
2015-11-01
Completion
2015-12-01
First posted
2015-01-08
Last updated
2015-12-18

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02334046. Inclusion in this directory is not an endorsement.

Remifentanil for Smooth Emergence in Elderly Patients (NCT02334046) · Clinical Trials Directory