Clinical Trials Directory

Trials / Completed

CompletedNCT05935930

Postoperative Effects of Propofol Versus Sevoflurane Anesthesia

Postoperative Effects of Propofol Versus Sevoflurane Anesthesia During Elective Non-Cardiac Surgeries. A Randomized Clinical Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Damanhour Teaching Hospital · Other Government
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

Background: The choice of appropriate anesthetics is essential to protect brain function, decrease perioperative complications, and provide high-quality care, and better quality of life. Objectives: To compare the efficacy and safety of propofol versus sevoflurane in patients undergoing elective, non-cardiac operations under general anesthesia. Methods: This was a randomized (1:1), parallel, phase four clinical trial; carried out on 44 patients, who were candidates for elective, non-cardiac operations under general anesthesia at our hospital. Patients were randomly allocated into two equal groups in which anesthesia was maintained with propofol infusion in group P and sevoflurane inhalation in group S.

Conditions

Interventions

TypeNameDescription
DRUGPropofol 10 MG/ML InjectionPropofol infusion
DRUGSevoflurane Inhalation LiquidSevoflurane inhalation

Timeline

Start date
2021-12-01
Primary completion
2024-12-15
Completion
2024-12-15
First posted
2023-07-07
Last updated
2025-02-05

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05935930. Inclusion in this directory is not an endorsement.