Condition: Surgical Site Infection · Sponsor: Monash University
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 antimicrobial prophylaxis in patients undergoing cardiac surgery
This description comes directly from the study's public registry record.
Paige Druce, MSc(Epi) · 9903 0016 · paige.druce@monash.edu
Sarah Astbury · 9076 6071 · sarah.astbury@monash.edu
Always discuss trial participation with your own doctor first.
| UT Southwestern Medical Centre | Dallas, Texas, United States | Not Yet Recruiting |
| Westmead Hospital | Sydney, New South Wales, Australia | Recruiting |
| St George Hospital | Sydney, New South Wales, Australia | Active Not Recruiting |
| The Prince Charles Hospital | Brisbane, Queensland, Australia | Recruiting |
| Princess Alexandra Hospital | Brisbane, Queensland, Australia | Recruiting |
| St Andrew's War Memorial Hospital | Brisbane, Queensland, Australia | Active Not Recruiting |
| Royal Adelaide Hospital | Adelaide, South Australia, Australia | Recruiting |
| Flinders Medical Centre | Adelaide, South Australia, Australia | Recruiting |
| Flinders Private | Adelaide, South Australia, Australia | Recruiting |
| Royal Hobart Hospital | Hobart, Tasmania, Australia | Recruiting |
| The Alfred Hospital | Melbourne, Victoria, Australia | Recruiting |
| The Royal Melbourne Hospital | Melbourne, Victoria, Australia | Recruiting |
+ 15 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05447559