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Status unknownNCT04775238Updated Mar 3, 2021

Effect of Metallic Nanoparticles on Nosocomial Bacteria

An interventional study of Silver nanoparticles and Copper nanoparticles in Nosocomial Infections, sponsored by Sohag University. Status unknown at 1 site in Egypt. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2021-03-03.

Sponsored by Sohag University · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

This research aims to study the properties of metallic nanoparticles"MNPs" (silver nanoparticles "AgNps" and copper nanoparticles "CuNps") on the 2 most common nosocomial bacteria which are highly resistant to antibiotics including Staphylococcus aureus and Pseudomonas aeruginosa, to evaluate the growth inhibiting properties of MNPs on all bacterial isolates, to evaluate the biofilm inhibitory effect on biofilm forming bacterial isolates and the synergistic effect of these MNPs in combination with antibiotics on the antibiotic resistant isolates.

Read the detailed description

There is a rapid increase in the number of health care associated infections (HAIs) due to multi-drug resistant (MDR) bacterial strains which have a worse prognosis being associated with significant morbidity and mortality, particularly in critically ill patients. The main problem with MDR strains is their limited treatment options, posing a major challenge for health care providers.The increasing utilization and immense studies of nanoparticles have brought new perspectives towards new antimicrobial material that could hinder the MDR bacteria pandemic currently faced. Particularly, metallic nanoparticles exhibit strong biocidal properties on different bacterial species, including MDR bacteria. Another important aspect of the antimicrobial properties of metallic nanoparticles is their potential to eradicate or inhibit microbial biofilm formation, which is an important virulence factor in many localized chronic infections.

02

Conditions studied

  • Nosocomial Infections

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Keywords

  • Staphylococcus aureus
  • Pseudomonas
  • silver nanoparticles
  • copper nanoparticles
03

In context

Cross Infection

239 studies on the registry are indexed under Cross Infection; 48 are open to participants now.

This study's planned enrollment of 100 is below the median of 210 across 142 interventional studies indexed under Cross Infection.

Browse Cross Infection studies →

Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Urinary tract infections (UTI)
  • Surgical site infections (SSI)
  • Catheter related blood stream infection (CRBSI)
  • Infected burns
  • Chest infection

Exclusion criteria

Exclusion Criteria:

  • Patients less than 18 years.
  • Community acquired infections
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Active comparator
    Group 1 (Staphylococcus aureus)

    Staphylococcus aureus is an example of gram positive bacteria which is a strong biofilm producer and highly resistant to antibiotics. Staphylococcus aureus will be exposed to silver nanoparticles and copper nanoparticles separately to study their antibacterial and biofilm inhibiting properties and their synergistic effect in combination with antibiotics.

    Other: Silver nanoparticles · Other: Copper nanoparticles

  • Active comparator
    Group 2 (Pseudomonas aeruginosa )

    Pseudomonas aeruginosa is an example of gram negative bacteria which is a strong biofilm producer and highly resistant to antibiotics. Pseudomonas aeruginosa will be exposed to silver nanoparticles and copper nanoparticles separately to study their antibacterial and biofilm inhibiting properties and their synergistic effect in combination with antibiotics.

    Other: Silver nanoparticles · Other: Copper nanoparticles

Interventions

  • OtherSilver nanoparticles

    AgNPs (19±5 nm)

    Also known as: AgNPs

  • OtherCopper nanoparticles

    CuNPs (150-350 nm)

    Also known as: CuNPs

06

What researchers measure

Primary outcomes

  1. Measurement of the inhibition zone diameter by (mm) around wells containing silver nanoparticles on nutrient agar containing 105 cfu/ml (colony forming unit/ml) Staphylococcus aureus

    Well diffusion method

    Time frame: 24 hours

  2. Measurement of the inhibition zone diameter by (mm) around wells containing silver nanoparticles on nutrient agar containing 105 cfu/ml Pseudomonas

    Well diffusion method

    Time frame: 24 hours

  3. Measurement of the inhibition zone diameter by (mm) around wells containing copper nanoparticles on nutrient agar containing 105 cfu/ml Staphylococcus aureus

    disc diffusion method

    Time frame: 24 hours

  4. Measurement of the inhibition zone diameter by (mm) around wells containing copper nanoparticles on nutrient agar containing 105 cfu/ml Pseudomonas

    disc diffusion method

    Time frame: 24 hours

  5. Antibiofilm Activity:12 μg/mL of AgNPs will be added to 107 CFU/mL of Staph aureus. using a microtiter plate reader at 595 nm, biofilm scores: nonbiofilm forming (-), weak (+), moderate (++), and strong (+++)

    Modified Tissue Culture Plate method (TCP):by ELISA

    Time frame: 24 hours

  6. Antibiofilm Activity:12 μg/mL of CuNPs will be added to 107 CFU/mL of Staph aureus. using a microtiter plate reader at 595 nm, biofilm scores: nonbiofilm forming (-), weak (+), moderate (++), and strong (+++)

    Modified Tissue Culture Plate method (TCP):by ELISA

    Time frame: 24 hours

  7. Antibiofilm Activity:12 μg/mL of AgNPs will be added to 107 CFU/mL of Pseudomonas. Using a microtiter plate reader at 595 nm, biofilm scores: nonbiofilm forming (-), weak (+), moderate (++), and strong (+++)

    Modified Tissue Culture Plate method (TCP):by ELISA

    Time frame: 24 hours

  8. Antibiofilm Activity:12 μg/mL of CuNPs will be added to 107 CFU/mL of Pseudomonas. Using a microtiter plate reader at 595 nm, biofilm scores: nonbiofilm forming (-), weak (+), moderate (++), and strong (+++)

    Modified Tissue Culture Plate method (TCP):by ELISA

    Time frame: 24 hours

  9. Synergism with antibiotics: cefoxitin, Tetracyclin, Ciprofloxacin, Rifampin, Linezolide impregnated with 42.5 μg/mL AgNPs will be placed on nutrient agar containing 105 cfu/ml of Staph aureus. Inhibition zones will be measured (mm).

    disc diffusion method

    Time frame: 24 hours

  10. Synergism with antibiotics: cefoxitin, Tetracyclin, Ciprofloxacin, Rifampin, Linezolide impregnated with 85 μg/mL CuNPs will be placed on nutrient agar containing 105 cfu/ml of Staph aureus. Inhibition zones will be measured (mm).

    disc diffusion method

    Time frame: 24 hours

  11. Synergism with antibiotics:piperacillin-tazobactam, Aztreonam, Imipenem, Colistin, Ciprofloxacin impregnated with 42.5 μg/mL AgNPs will be placed on nutrient agar containing 105 cfu/ml of Pseudomonas. Inhibition zones will be measured (mm).

    disc diffusion method

    Time frame: 24 hours

  12. Synergism with antibiotics:piperacillin-tazobactam, Aztreonam, Imipenem, Colistin ,Gentamicin, Ciprofloxacin impregnated with 85 μg/mL CuNPs will be placed on nutrient agar containing 105 cfu/ml of Pseudomonas. Inhibition zones will be measured (mm).

    disc diffusion method

    Time frame: 24 hours

07

Study locations

1 of 1 sites recruiting
  • Faculty of medicine - sohag university
    Sohag, 82524, Egypt
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04775238
Lead sponsor
Sohag University
Responsible party
Nahed Fathallah Fahmy (lecturer of medical microbiology & immunology departement -faculty of medicine- sohag university, Sohag University) — Principal investigator
First posted
Mar 1, 2021
Start date
Feb 27, 2021
Primary completion
Jun 20, 2021 (estimated)
Completion
Jul 1, 2021 (estimated)
Last update
Mar 3, 2021

Study contacts

Nahed Fathallah, lecturer
Contact
nanafahmy_783@yahoo.com
01142283865
Ekram Abdelrahman, lecturer
Contact
dr.ekram.ar@gmail.com
+201004691692
Nahed Fathallah, lecturer
principal investigator · Sohag University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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