Completed

Antimicrobial Resistance Predictors in Respiratory ICU Patients

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: October 2024
See protocol details

Summary

Principal SponsorMohamed Sabry
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2024

Actual date on which the first participant was enrolled.

The goal of this clinical trial is to identify the predictors of antibiotic resistance like the history of previous antibiotic ,the antibiogram of the centre , comorbidities,..etc to decide the suitable antibiotic

Official TitlePredictors of Antimicrobial Resistance in the Respiratory Intensive Care Unit of Alexandria Main University Hospital
NCT06750744
Principal SponsorMohamed Sabry
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: * Adult patient admitted to the respiratory ICU due to bacterial infection. * Recent antibiotic intake in the past three months. * Intercostal tube insertion for empyema. * Shocked patients with inserted central venous catheter. * Intubated or tracheostomized patients. * Patients with grade two to four bed sores. Exclusion Criteria: * . Inability to provide written informed consent for the study. * Non sterile sample collection technique. * Inability to provide antibiogram. * Isolated patients due to suspected tuberculosis

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Chest Department -Faculty of Medicine

Alexandria, EgyptOpen Chest Department -Faculty of Medicine in Google Maps
CompletedOne Study Center