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Clinical Trials in Egypt / NCT07475429
Starting soon Observational

Impact of Siderophore Genes on Cefiderocol Susceptibility in Carbapenem Resistant Hypervirulent Klebsiella Pneumoniae

NCT07475429 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-03-15
Last updated
2026-03-24

Condition(s) studied

Carbapenem-resistant Hypervirulent Klebsiella Pneumoniae Infection

Investigational drug(s) / intervention(s)

Cefiderocol susceptibility testing

Cefiderocol susceptibility testing: Determination of cefiderocol susceptibility in carbapenem-resistant hypervirulent Klebsiella pneumoniae isolates using antimicrobial susceptibility testing according to CLSI guidelines.

Study summary

1. Sample: Clinical specimens (blood, urine, sputum, wound swabs) will be collected aseptically and transported to the microbiology laboratory for analysis.
2. Culture: Specimens will be inoculated on MacConkey agar and incubated at 35-37°C for 18-24 hours. Colonies with typical K. pneumoniae morphology (mucoid, lactose-fermenting) will be selected for further testing
3. Identification of isolates will be done by:

Colony morphology, Gram staining, and conventional biochemical tests (eg, indole, citrate utilization, urease, Voges-Proskauer) .
4. Antimicrobial susceptibility testing of the isolates :

Antimicrobial susceptibility testing was performed and interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guidelines, M100 document (latest edition)."
5. MIC determination for cifederecol using E-test .
6. Phenotypic Detection of hvKP:

1. String Test: A viscous string ≥5 mm formed by stretching a single colony indicates hypermucoviscosity .
2. Capsule Staining: to visualize large capsules .
3. Siderophore Production: Assessed on chrome azurol S (CAS) agar to detect iron-chelating activity.
7. Detection of siderophore genes by Simple qualitative PCR .

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: \- 1. Patients with hypervirulant K. pneumoniae infection from various clinical specimens (blood, urine, sputum, wound swabs, etc.) Confirmed by culture and initial laboratory testing . 2\. Age and sex range: any age and any sex. Exclusion Criteria: \- Patients who received antibiotic treatment in the 48 hours prior to sample collection. 2\. Patients with incomplete clinical data or inadequate samples.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Medicine Sohag Egypt

More Sohag University trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07475429 on ClinicalTrials.gov ↗ ← All trials in Egypt