Predictors of Antimicrobial Resistance in the Respiratory Intensive Care Unit of Alexandria Main University Hospital
1 other identifier
observational
50
1 country
1
Brief Summary
The goal of this clinical trial is to identify the predictors of antibiotic resistance whether clinical or laboratory or radiological or all
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 11, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 12, 2024
CompletedFirst Submitted
Initial submission to the registry
December 20, 2024
CompletedFirst Posted
Study publicly available on registry
December 27, 2024
CompletedDecember 27, 2024
December 1, 2024
2 months
December 20, 2024
December 24, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
antibiogram
resistance rates in antibiograms
3 months
Other Outcomes (1)
resistance rates in the antibiogram
3 months
Study Arms (1)
only one group of patients
to identify the predictors of antibiotic resistance using rates of resistance,comprehensive data of each patient chest X ray,CT,ultrasound
Interventions
chest X ray identify severity of pneumonia
Eligibility Criteria
The current study aims to identify the predictors of antibiotic resistance in the respiratory intensive care unit of Alexandria main university hospital
You may qualify if:
- 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.
You may not qualify if:
- Inability to provide written informed consent for the study.
- Non sterile sample collection technique.
- Inability to provide antibiogram.
- Isolated patients due to suspected tuberculosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mohamed Sabrylead
Study Sites (1)
Chest Department -Faculty of Medicine
Alexandria, Azarita, 11511, Egypt
Related Links
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
mohamed sabry eltarhony, lecturer
Alexandria University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Lecturer of chest diseases
Study Record Dates
First Submitted
December 20, 2024
First Posted
December 27, 2024
Study Start
October 1, 2024
Primary Completion
December 11, 2024
Study Completion
December 12, 2024
Last Updated
December 27, 2024
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share
because the facility, where i do my work, refuse to share any project untill it is fully published