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
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol 10 MG/ML Injection | Propofol infusion |
| DRUG | Sevoflurane Inhalation Liquid | Sevoflurane 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.