Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT03581370

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

Led by University Hospital, Toulouse · Updated on 2024-09-25

80

Participants Needed

1

Research Sites

332 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with ventilator-associated pneumonia caused by Pseudomonas aeruginosa
  • Hospitalized in intensive care units
  • Pseudomonas aeruginosa susceptible to ceftolozane-tazobactam
  • Simplified Acute Physiological Score II (SAPS II) greater than 20
  • Expected survival longer than 7 days
  • Informed consent obtained from patient or authorized representative
  • Affiliated to a social security scheme or equivalent
Not Eligible

You will not qualify if you...

  • History of allergy to ceftolozane-tazobactam or beta-lactam antibiotics
  • Infection caused by strains resistant to ceftolozane-tazobactam
  • Renal insufficiency with glomerular filtration rate less than 50 ml/min
  • On dialysis or receiving continuous hemodiafiltration
  • Pregnant or breastfeeding women
  • Under legal protection for adults
  • Active immunodepression

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Service Réanimation Polyvalente - CHU Rangueil

Toulouse, France, 31059

Actively Recruiting

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Research Team

S

Stéphanie RUIZ, MD

CONTACT

N

Nathalie ROQUES

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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