About this trial
This observational study compares extended versus intermittent beta-lactam infusion in sepsis patients, assessing survival, clinical cure rates, and practical ICU challenges. The findings will guide optimal antibiotic protocols, potentially improving sepsis outcomes through precision dosing strategies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged: 18 - 65
Temperature: over 38 degree celsius
Heart rate: over 100 beats per minute
Respiratory rate: over 20 breaths per minute
Disqualifiers
Hypersensitivity to Beta-lactams
Pregnancy
Very low probability of survival using APAACHE II score > 34 points.
Immunodeficency or taking immunosuppressive medications
Trial population
Critically ill patient diagnosed with pneumonia at Critical care unit at Assiut University Hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
Extended beta-lactam antibiotics
DrugGroup A will be receiving extended infusion of beta-lactam antibiotic over 4 hours.
Intermittent Beta-lactam antibiotics
DrugGroup B will be receiving intermittent infusion of beta-lactam antibiotic over 30 minutes.
Treatment groups
Trial outcomes
Primary outcomes
All-cause mortality at 28 days from the date of randomization.
Secondary outcomes
Clinical cure
defined as completing the full course of beta-lactam therapy within 14 days without requiring additional antibiotics for the same infection within 48 hours after treatment cessation.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
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