This is a sub-study of the S. aureus Network Adaptive Platform (SNAP) trial (NCT05137119) wherein we will evaluate whether not giving rifampin in patients with probable or definite prosthetic valve endocarditis due to S. aureus is non-inferior to giving rifampin.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
330
Patients will receive rifampin 900mg a day in 2-3 divided doses
Subjects will be assigned to not receive adjunctive rifampin
McGill University Health Centre (Royal Victoria Hospital and Montreal General Hospital)
Montreal, Quebec, Canada
RECRUITINGTreatment failure
A composite outcome of all cause mortality, unplanned cardiac surgery, new cardioembolic events, or relapse of bacteremia due to S. aureus.
Time frame: 180 days
All-cause mortality
Death due to any cause
Time frame: 180 days
Unplanned cardiac surgery
The need for cardiac surgery which was not planned or scheduled at the time of randomization.
Time frame: 180 days
New embolic events
A new symptomatic cardio-embolic event occurring after randomization.
Time frame: 180 days
Relapse of bacteremia
A new S. aureus bacteremia with the same susceptibility pattern (except for quinolones or rifampin in those who are exposed) which develops after sterilization of the initial blood cultures
Time frame: 180 days
Discontinuation of rifampin due to new drug-drug interaction
The cessation of adjunctive rifampin due to a new pharmacologically significant drug-drug interaction.
Time frame: 56 days
Serious adverse drug reaction due to rifampin
Patients who have a CTCAE grade 4 reaction which is determined by expert adjudication to be probably or definitely due to rifampin.
Time frame: 56 days
Discontinuation of rifampin due to an adverse drug reaction
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Any adverse drug reaction which leads to the discontinuation of rifampin
Time frame: 56 days