Duration of Cardiac Antimicrobial Prophylaxis Outcomes Study
Recruiting
Phase 4
Interventional Study
Surgical Site Infection
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 9,180 (estimated)
- Sponsor
- Monash University · Other
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About This Trial
This multicentre, adaptive, pragmatic, double-blind, three-arm, placebo-controlled, randomised, non-inferiority clinical trial will compare the incidence of surgical site infection and other healthcare associated infections, health economic and microbiological impact after intraoperative only (Arm A), to 24 hours (Arm B) and, to 48 hours (Arm C) of IV cefazolin and placebo postoperative surgical a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
\- Adult patients undergoing cardiac surgery involving a median sternotomy
Exclusion Criteria:
* Age \<18 years
* American Society of Anesthesiology (ASA) 5
* Subjects with GFR \<40mL/min/1.73m2 or those requiring continuous renal replacement therapy, haemodialysis or peritone…
Contacts