Clinical Trials Directory

Trials / Completed

CompletedNCT04773002

A Comparison of Volatile Anesthesia and Total Intravenous Anesthesia (TIVA)

A Comparison of Volatile Anesthesia and Total Intravenous Anesthesia (TIVA) on Ecchymosis, Edema, and Intraoperative Bleeding in Rhinoplasty

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

Summary

In this study, investigators wanted to investigate the effect of volatile anesthesia and total intravenous anesthesia (TIVA) on ecchymosis, edema, and intraoperative bleeding in rhinoplasty.

Detailed description

Routine monitorization (blood pressure, pulse, oxygen saturation with pulse oximetry and electrocardiogram) will be applied to all patients taken into the operation room. In Group P (TIVA), induction of anesthesia will be achieved with 2 mg/kg propofol, 0.6 mg/kg rocuronium, and 1 μ / kg fentanyl. Propofol and remifentanil will be used in the continuation of anesthesia. In Group S (Volatile), anesthesia will be induced with 2 mg / kg propofol, 0.6 mg / kg rocuronium and 1 μ / kg fentanyl. 50% nitrous oxide + 50% oxygen and 2% sevoflurane will be used in the continuation of anesthesia. All patients will receive 2 ml/kg/hour Ringer's lactate solution during the operation.

Conditions

Interventions

TypeNameDescription
OTHERDifferent anesthesia methodsTotal intravenous anesthesia (TIVA)and volatile anesthesia

Timeline

Start date
2021-03-18
Primary completion
2021-08-21
Completion
2021-08-21
First posted
2021-02-26
Last updated
2022-03-16

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04773002. Inclusion in this directory is not an endorsement.