Efficacy of Optimized Antimicrobial Combination Therapy for Treatment of Enterococcus Faecalis Bacteremia and Identification of Intestinal Microbiota Signature

Status: Recruiting
Location: See all (4) locations...
Study Type: Observational
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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, gentamycin, streptomycin), at common suggested dosages for EF-BSI in empirical or definitive therapy

• Written informed consent

Locations
Other Locations
Italy
IRCCS Azienda Ospedaliero-Universitaria di Bologna
RECRUITING
Bologna
Ospedale Maggiore Carlo Alberto Pizzardi di Bologna
RECRUITING
Bologna
Azienda Ospedaliero Universitaria di Catanzaro Mater Domini
RECRUITING
Catanzaro
Humanitas Research Hospital
RECRUITING
Milan
Contact Information
Primary
Maddalena Giannella, MD PhD
maddalena.giannella@unibo.it
+39 0512143199
Time Frame
Start Date: 2021-02-06
Estimated Completion Date: 2026-09-26
Participants
Target number of participants: 510
Treatments
Adult with Enterococcus faecalis monomicrobial bloodstream infection
Adult patients with primary Enterococcus faecalis monomicrobial bloodstream infection
Related Therapeutic Areas
Sponsors
Leads: IRCCS Azienda Ospedaliero-Universitaria di Bologna

This content was sourced from clinicaltrials.gov