Overview

Short Infusion Versus Prolonged Infusion of Ceftolozane-tazobactam Among Patients With Ventilator Associated-pneumonia

Status:
Recruiting
Trial end date:
2023-02-01
Target enrollment:
0
Participant gender:
All
Summary
The main objective of this study is to compare the median exposures at pharmacokinetic equilibrium of the two modalities of administration: 4-hours infusion of ceftolozane-tazobactam at a dosage of 2 gram three times a day vs 1-hour infusion of 2 gram three times a day.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Hospital, Toulouse
Treatments:
Ceftolozane, tazobactam drug combination
Cephalosporins
Penicillanic Acid
Pharmaceutical Solutions
Tazobactam
Criteria
inclusion criteria

- patients with ventilator associated-pneumonia to Pseudomonas aeruginosa

- patients hospitalized in intensive care units

- Pseudomonas aeruginosa susceptible to ceftolozane-tazobactam

- Simplified Acute Physiological Score II (SAPS II () > 20

- Expected duration of survival > 7 days

- Informed consent of the patient or, failing that, the patient's close or trustworthy
person

- Affiliated to a social security scheme or equivalent

Non inclusion criteria:

- history of allergy to one of the two molecules

- history of allergy to betalactamines

- Strain Isolated resistant to Ceftolozane-Tazobactam combination

- Renal insufficiency with a glomerular filtration rate evaluated by Chronic Kidney
Disease Epidemiology Collaboration (CKD-EPI) < 50 ml/min

- Patient on dialysis or under continuous hemodiafiltration

- pregnant or nursing women

- patient benefiting from a system of legal protection for adults

- patient with active immunodepression.