Clinical Trials Directory

Trials / Completed

CompletedNCT04394897

Total Intravenous Anesthesia With Remifentanil-propofol Admixture

Total Intravenous Anesthesia With Remifentanil-propofol Admixture Using Single-infusion Technique

Status
Completed
Phase
Study type
Observational
Enrollment
96 (actual)
Sponsor
Bezmialem Vakif University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Background: Application of total intravenous anesthesia (TIVA) may be considered as unpractical when compared with inhalational anesthesia. Although it is mostly not recommended, mixing intravenous agents seems to be popular in clinical practice. The aim of the study was to investigate the possible clinical drawbacks of using remifentanil-propofol admixture (MIXTIVA) for TIVA.

Detailed description

ASA I-II adult patients scheduled for elective thyroidectomy were randomly allocated into 3 groups (n= 32 for each) to have TIVA either with remifentanil and propofol infusions separately (control group, Group I) or with MIXTIVA infusion that had remifentanil/propofol proportion 2/1000 or 3/1000 (remifentanil concentration 20 µg/ml or 30 µg/ml in propofol 1%, Group II or Group III respectively). This technique may be considered as a practical implementation for busy ambulatory surgery centers performing general anesthesia, but delayed recovery may be predicted with longer duration of surgery and anesthesia.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTRemifentanil-Propofol admixture

Timeline

Start date
2013-03-12
Primary completion
2014-04-12
Completion
2014-04-12
First posted
2020-05-20
Last updated
2020-05-20

Source: ClinicalTrials.gov record NCT04394897. Inclusion in this directory is not an endorsement.