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NCT04773002 Clinical Trial

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 Details — Status: Completed

Administrative data
NCT number NCT04773002
Other study ID # 21-KAEK-006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 18, 2021
Est. completion date August 21, 2021

Study information
Verified date March 2022
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 52
Est. completion date August 21, 2021
Est. primary completion date August 21, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Between 18 and 65 years - Planned to rhinoplasty - An American Society of Anesthesiologists score of 1 or 2 Exclusion Criteria: - Steroid use - Patients with coagulation disorders, •Rejected to participation

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Different anesthesia methods
Total intravenous anesthesia (TIVA)and volatile anesthesia

Locations
Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)
Lead Sponsor Collaborator
Tokat Gaziosmanpasa University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Edema and ecchymosis in rhinoplasty according to the type of anesthesia. It is evaluation developing edema and ecchymosis according to total intravenous anesthesia and volatile anesthesia in rhinoplasty. one time in six months
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