drugset / Trial / NCT07148960

Does Staphylococcus Aureus Bacteremia Early Dual Therapy Improve Outcomes?

NCT07148960

Phase 4 Enrolling by invitation 300 enrolled West Virginia University
RandomizedParallel-groupOpen-labelTreatment

Summary

The goal of this open-label, pragmatic, randomized controlled clinical trial is to learn if patients with Staphylococcus aureus bacteremia (SAB) given the intervention of early dual intravenous (IV) antibiotic therapy will decrease duration of bacteremia (\< 6 days) and improve outcomes compared to single IV antibiotic therapy. The main questions this study aims to answer are: * To decrease SAB duration and improve outcomes by using early dual vs. single agent IV antibiotic therapy * To accelerate practice transformation of earlier IV to oral (PO) antibiotic transition by switching to PO antibiotic therapy once blood cultures are negative at 72 hours Participants will be asked to agree to be randomized (like flipping a coin) to receive two or one IV antibiotic(s). Once the infection has cleared, the treatment will be changed to PO antibiotics. As part of usual care, participants will have weekly lab tests for monitoring while on antibiotics, receive a telephone call to see how the participants are doing, and follow up in person or by telephone or video in Infectious Diseases (ID) Clinic. Participant participation will last 12 weeks after the participant is discharged from the hospital.

Timeline

Start
2025-09-15
Primary completion
2027-07
Completion
2027-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cefazolin Small molecule Intravenous
Subject Ceftaroline Other / unclassified Intravenous
Subject Daptomycin Other / unclassified Intravenous
Subject Ertapenem Small molecule Intravenous
Comparator Vancomycin Other / unclassified Intravenous
Comparator nafcillin Small molecule Intravenous
Comparator oxacillin Small molecule Intravenous
Background Rifampin Small molecule Oral