Combination Cefazolin With Ertapenem for Methicillin-susceptible Staphylococcus Aureus Bacteremia (CERT)

Who is this study for? Patients with methicillin-susceptible staphylococcus aureus bacteremia
What treatments are being studied? Cefazolin+Ertapenem
Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

There is a variety of in vitro, in vivo (animal model), and human case series data which suggests that the addition of ertapenem to cefazolin could improve outcomes in methicillin-susceptible S. aureus bacteremia. No randomized controlled trial has been performed. This study is an approved sub-study of The Staphylococcus aureus Network Adaptive Platform (SNAP) trial (NCT05137119)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Adult \>=18 years old

• S. aureus bacteremia within the past 48 hours:

‣ with any unknown MRSA status (in centers with \<15% prevalence of MRSA in their annual blood cultures) or known negative MRSA screening swab within 90 days OR

⁃ which has already been shown to be MSSA

• Current receipt of cefazolin or where it would be clinically appropriate (according to treating ID specialist) to switch to cefazolin as the backbone therapy (open label, non-study drug).

∙ NOTE: Up to an additional 12-24 hours of open label non-study VANCOMYCIN, LINEZOLID or DAPTOMYCIN may be allowed if there is sepsis and clinical concern for MRSA has not been excluded.

Locations
Other Locations
Canada
Foothills Medical Centre
RECRUITING
Calgary
Hamilton Health Sciences (Hamilton General Hospital and Juravinski Hospital)
RECRUITING
Hamilton
Hospital de la Cité de la Sante
RECRUITING
Laval
McGill University Health Centre (Royal Victoria Hospital and Montreal General Hospital)
RECRUITING
Montreal
Niagara Health - Niagara Falls Site
RECRUITING
Niagara Falls
Contact Information
Primary
Lina Petrella
lina.petrella@muhc.mcgill.ca
514-934-1934
Time Frame
Start Date: 2024-05-20
Estimated Completion Date: 2026-07
Participants
Target number of participants: 60
Treatments
Experimental: Ertapenem
Ertapenem 1g IV daily infused over 2 hours x 5 days
Placebo_comparator: Placebo
Saline placebo infused daily over 2 hours x 5 days
Related Therapeutic Areas
Sponsors
Leads: Todd C. Lee MD MPH FIDSA

This content was sourced from clinicaltrials.gov