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

Hemorrhage Clinical Trial

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

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04773002
Study type Observational [Patient Registry]
Source Tokat Gaziosmanpasa University
Contact
Status Completed
Phase
Start date March 18, 2021
Completion date August 21, 2021
View Details
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