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Enrolling By Invitation NCT07148960

Does Staphylococcus Aureus Bacteremia Early Dual Therapy Improve Outcomes?

Conditions: Staphylococcus Aureus Bacteremia

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 300
Sponsor: West Virginia University

Location: West Virginia University Morgantown West Virginia

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.

Eligibility Criteria

Inclusion Criteria: * The patient is hospitalized at J.W. Ruby Memorial Hospital, Berkeley Medical Center, Camden Clark Medical Center, Princeton Community Hospital, United Hospital Center, or Wheeling Hospital * The patient has been identified to have Staphylococcus aureus bacteremia * The patient is able to participate in lab monitoring and in-person or telemedicine ID Clinic follow-up Exclusion Criteria: * The patient or an appointed medical decision maker is unable to give informed consent * The patient is a prisoner, pregnant, and/or mentally handicapped * The patient is determined unsafe for enrollment at the primary team's discretion

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07148960). StuddyBuddy aggregates publicly available trial information.