- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06628076
Antibacterial Effect of Zinc Oxide Nanoparticles on Acinetobacter Baumannii Isolated from Patients with Hospital Acquired Infections in Sohag University Hospitals, Egypt
Study Overview
Status
Detailed Description
Acinetobacter baumannii (A. baumannii) is Gram- negative, aerobic, glucose non-fermentative, non-motile coccobacillus, ubiquitous in nature, and persistent in healthcare settings. It is regarded as a significant opportunistic human pathogen.
This bacterium become a growing problem in hospitals as a predominant multidrug-resistant (MDR) bacterium. Horizontal acquisition of resistance genes is the main factor involved in the emergence of MDR .
There are many mechanisms to confer resistance to different classes of antibiotics in A. baumannii, one of them is multidrug efflux pumps. These efflux pumps are important source of MDR, which export antibiotics from the cell, increasing their antibiotic resistance.
AdeABC is one of the most important efflux systems, belonging to the RND family in Acinetobacter, which plays an important role in the resistance to a broad group of antibiotics; its genes are chromosomal and encode three genes, i.e., AdeB, AdeA, and AdeC, forming an operon in the vicinity. In addition, the expression of AdeABC is done by a two-component system, which includes a response regulator (AdeR) and a sensor kinase (AdeS) .
The ability of Acinetobacter spp. to form biofilm that enables bacterial survival in hospital settings, especially in ICUs, is the most significant contributing factor to their virulence, and this trait is also responsible for their notable antibiotic resistance. Several biofilm-related genes influence antimicrobial susceptibility, suggesting an association between the biofilm-forming ability of Acinetobacter spp. and their antibiotic resistance patterns (MDR/XDR)
Zinc oxide nanoparticles (ZnO NPs) are one of the most important nanoparticles of metal oxides; it is a unique and inorganic materials that can be used in several biological applications (anti-bacterial, anti-inflammatory). ZnO NPs exhibit distinctive properties other than other nanoparticles such as higher solubility, better biofilm penetration and effective drug delivery . ZnO NPs have been reported to have antimicrobial properties such as disrupting the cell membrane of pathogens, accumulating in the cell and producing toxic H2O2 (hydrogen peroxide)
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Shimaa Anwar Ahmed, Assistant Lecturer
- Phone Number: +201092533978
- Email: shaymaa_abdelgaber@med.sohag.edu.eg
Study Contact Backup
- Name: Noha Saber Shafik, lecturer
- Email: Nohasaber@med.sohag.edu.eg
Study Locations
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-
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Sohag, Egypt, 534568
- Sohag University, Faculty of Medicine
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Contact:
- sohag University, professor
- Phone Number: 0201009222054
- Email: Sohaguniversity@med.sohag.edu.eg
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Contact:
- Mona Fatooh mohmad, professor
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Contact:
- Noha Saber Shafik, lecturer
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Contact:
- Mohammed Ahmed Mahmoud, lecturer
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Contact:
- Shimaa Anwar Ahmed, lecturer
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients suffering from infections that can be caused by A. baumannii.
Exclusion Criteria:
- All patients suffering from infections that aren't caused by A. baumannii.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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A. baumannii antibiotic susceptibility profile
Time Frame: October 2024 to December 2025
|
A. baumannii antibiotic susceptibility profile will be done using modified kirbybeur method
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October 2024 to December 2025
|
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Isolation and identification of A. baumannii from different clinical samples
Time Frame: October 2024 to December 2025
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Isolation and identification of A. baumannii from different clinical samples using MacConKey medium, oxidase test.
TSI, And automated identification ViteK system
|
October 2024 to December 2025
|
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A. baumannii strains which produce biofilm
Time Frame: October 2024 to December 2025
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Detection of A. baumannii strains which produce biofilm using tissue culture plates and Gram stain
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October 2024 to December 2025
|
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Ability of ZnO NPs to inhibit the phenomenon of biofilm formation by MDR A. baumannii strains
Time Frame: October 2024 to December 2025
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Assessment of ability of ZnO NPs to inhibit the phenomenon of biofilm formation by MDR A. baumannii strains using ZnO NPs to be applied by different concentrations on tissue culture plates and measure the degree of Biofilm formation using ELISA
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October 2024 to December 2025
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The effect of ZnO NPs on the expression of some efflux pump genes and biofilm related genes in MDR A. baumannii strains
Time Frame: October 2024 to December 2025
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Evaluation the effect of ZnO NPs on the expression of some efflux pump genes and biofilm related genes in MDR A. baumannii strains using real time PCR(Polymerase Chain reaction)
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October 2024 to December 2025
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Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Respiratory Tract Diseases
- Disease Attributes
- Iatrogenic Disease
- Infections
- Communicable Diseases
- Respiratory Tract Infections
- Cross Infection
- Physiological Effects of Drugs
- Anti-Infective Agents
- Protective Agents
- Dermatologic Agents
- Antitubercular Agents
- Radiation-Protective Agents
- Sunscreening Agents
- Anti-Bacterial Agents
- Antibiotics, Antitubercular
- Zinc Oxide
Other Study ID Numbers
- Soh-Med-24-9-1MD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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