BetaLACTA® Test for Early De-escalation of Empirical Carbapenems in Pulmonary, Urinary and Bloodstream Infections in ICU

NACompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

October 20, 2017

Primary Completion Date

September 21, 2019

Study Completion Date

October 20, 2019

Conditions
PneumoniaUrinary Tract InfectionsBloodstream Infection
Interventions
DEVICE

betaLACTA® rapid diagnostic test

Since ≥1 bacteriological sample(s) from ICU patients empirically treated with carbapenems (i.e. respiratory sample such as quantitative tracheobronchial aspirate with available volume ≥1 mL; urinary sample such as single catheter urine specimen; or blood culture) is positive for ≥2 GNB/field on direct examination, empirical carbapenem will be adapted: 1) early, since the second dose, according to the results of the betaLACTA® rapid diagnostic test (BLT) in the intervention arm (i.e. de-escalation to cefepim or to ceftazidim+amikacin in case of negativity, and carbapenem continuation in case of positivity); or 2) after 48-72h according to the results of the antibiotic susceptibility test in the control arm.

Trial Locations (1)

75020

Anesthesiology and Critical Care Medicine Department, Paris

All Listed Sponsors
lead

Assistance Publique - Hôpitaux de Paris

OTHER

NCT03147807 - BetaLACTA® Test for Early De-escalation of Empirical Carbapenems in Pulmonary, Urinary and Bloodstream Infections in ICU | Biotech Hunter | Biotech Hunter