Impact of a Strategy Based on Bacterial DNA Detection to Optimize Antibiotics in Immunocompromised Patients With Hospital-acquired Pneumonia Requiring Mechanical Ventilation

Recruiting N/A Interventional Study
Pneumonia, Ventilator-Associated Pneumonia, Hospital-Acquired Immunodeficiency
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
31 (estimated)
Sponsor
University Hospital, Lille · Other
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About This Trial
RESPIRE is a randomized, unblinded, controlled study to measure the impact of a strategy based on a PCR test on the adjustment of antimicrobial therapy in immunocompromised patients suspected with ventilator-associated or hospital-acquired pneumonia (VAP/HAP) requiring mechanical ventilation (MV) in Intensive Care Unit (ICU). The gold-standard microbiological diagnostic method for pneumonia in the…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult immunocompromised patients hospitalized in ICU with suspected VAP or HAP requiring MV Exclusion Criteria: * No immunodeficiency Moribund patients (SAPS II \> 90) Pregnant women Refuse to participate to the study
Contacts

Marion HOUARD, MD

0320445962

marion.houard@chru-lille.fr

CONTACT