Antimicrobial Combination Therapy for Treatment of Enterococcus Faecalis Bacteremia

Recruiting Observational Study
Enterococcus Faecalis Infection Blood Stream Infection Gut Microbiomes
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
510 (estimated)
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna · Other
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About This Trial

Prospective, multicenter, national, observational pharmacological study on the evaluation of efficacy of appropriate monotherapy vs combination treatment for non-complicated Enterococcus faecalis (EF) bloodstream infection (BSI) and identification of gut microbiota fingerprint of patients with EF-BSI correlated to antimicrobial treatment and clinical outcome

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult (≥18 years) * Monomicrobial EF-BSI * Receipt of ≥ 5 days of at least one in vitro active drug (ampicillin, amoxicillin/clavulanate, ampicillin/sulbactam, piperacillin, vancomycin, teicoplanin, daptomycin and linezolid) with or without a synergistic drug (ceftriaxone, gen…
Contacts

Maddalena Giannella, MD PhD

+39 0512143199

maddalena.giannella@unibo.it

CONTACT