Predictors of Antimicrobial Resistance in the Respiratory Intensive Care Unit of Alexandria Main University Hospital
NCT ID: NCT06750744
Last Updated: 2024-12-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
50 participants
OBSERVATIONAL
2024-10-01
2024-12-12
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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
chest x ray
chest X ray identify severity of pneumonia
chest X ray
chest radiological evaluation via x ray
Tigecycline (Tygacil)
selective antibiogram
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
chest x ray
chest X ray identify severity of pneumonia
chest X ray
chest radiological evaluation via x ray
Tigecycline (Tygacil)
selective antibiogram
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* Non sterile sample collection technique.
* Inability to provide antibiogram.
* Isolated patients due to suspected tuberculosis
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mohamed Sabry
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohamed Sabry
Lecturer of chest diseases
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
mohamed sabry eltarhony, lecturer
Role: PRINCIPAL_INVESTIGATOR
Alexandria University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chest Department -Faculty of Medicine
Alexandria, Azarita, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Study Documents
Access uploaded study-related documents such as protocols, statistical analysis plans, or lay summaries.
Document Type: Study Protocol
View DocumentRelated Links
Access external resources that provide additional context or updates about the study.
antimicrobial resistancde prediction
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AMR-AMUH
Identifier Type: -
Identifier Source: org_study_id