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Clinical Trials/NCT06739382
NCT06739382
Completed
Phase 3

Management of Ventilation Acquired Pneumonia Caused by Pseudomonas and Acinetobacter Organisms in a Pediatric Center: a Randomized Controlled Study

Beni-Suef University1 site in 1 country64 target enrollmentJanuary 1, 2021

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Ventilation Acquired Pneumonia
Sponsor
Beni-Suef University
Enrollment
64
Locations
1
Primary Endpoint
Antimicrobial susceptibility
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to determine the most effective empirical therapy of antibiotics for better ventilator-associated pneumonia control. The main question it aims to answer is:

• Which is better for clinical response single or combination empiric antibiotic therapies ?

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
January 1, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hasnaa Osama

Beni-Suef University

Beni-Suef University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Antimicrobial susceptibility

Time Frame: 7 days

Antimicrobial susceptibility was assessed through Kirby-Bauer's disc diffusion method (DD), Minimal Inhibitory Concentration (MIC) using the automated VITEK 2 compact system (bioMérieux, France), and the Ameri-Ziaei Double Antibiotic Synergism Test (AZDAST). Interpretation of DD and MIC results followed CLSI guidelines.

Study Sites (1)

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