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Efficacy and Safety of Prophylactic Antibiotics in Preventing Ventilator-associated Pneumonia: A Randomized, Double Blind, Placebo-controlled Trial

Efficacy and Safety of Prophylactic Antibiotics in Preventing Ventilator-associated Pneumonia: A Randomized, Double Blind, Placebo-controlled Trial

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07203638
Enrollment
100
Registered
2025-10-02
Start date
2024-11-01
Completion date
2025-11-01
Last updated
2025-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator-Associated Pneumonia (VAP)

Brief summary

Evaluate efficacy and safety of prophylactic antibiotics in preventing early ventilator-associated pneumonia

Interventions

Beta lactam cefipim infusion (20mg/kg -12h -2 days ) total volume 10 ml

DRUGSalin

Patient will receive .9 % saline (10ml /12h/2days)

Sponsors

Esraa Salah Mohamed Abdallah Eladl
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Intervention model description

Efficacy of prophylactic antibiotic against vent.associated pneumonia

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* • Age \> 18 years or older * Both sexes will be included. * Invasive mechanical ventilation

Exclusion criteria

* ongoing pneumonia or gross aspiration confirmed by the presence of lung infiltrates on chest radiographs at admission before invasive ventilation * previous lung disease precluding accurate interpretation of chest radiographs * ongoing antibiotic therapy or during the week before admission * known chronic colonization with multidrug-resistant bacteria * known allergy to beta-lactam antibiotics * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Ventilation associated pneumoniafrom the 2nd to the 7th day of mechanical ventilationThe primary outcome is the proportion of patients who will develop VAP (radiology, TLC, temperature, hemodynamic, sputum culture )from the 2nd to the 7th day of mechanical ventilation

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026