Efficacy of Cotrimoxazole as a De-escalation Treatment of Ventilator-Associated Pneumonia in Intensive Care Unit

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Efficacy of cotrimoxazole as a de-escalation treatment for adult patients Ventilator-Associated Pneumonia in intensive care unit Multicentre randomized non-inferiority trial comparing cotrimoxazole to standard antibiotic therapy for enterobacterial VAP

Eligibility criteria

Qualifiers

Adult patients hospitalized in an ICU

Under mechanical ventilation for at least five days

Microbiologically confirmed VAP preferably on a distal lung sample (bronchoalveolar lavage or protected distal specimen) otherwise endotracheal aspiration

Enterobacteriaceae susceptible to cotrimoxazole, and for polymicrobial VAP, all bacteria susceptible to cotrimoxazole

Disqualifiers

Haemodynamic instability (increasing dose of a catecholamine in the last 24 hours)

allergy,

advanced liver insufficiency,

renal dysfunction with clearance <15 mL/min/1.73 m² without hemodialysis

Trial design

Treatments tested in this trial

  • cotrimoxazole
  • standard antibiotic therapy

Treatment groups

628 Participants
are divided into 2 treatment groups