drugset / Trial / NCT05447559

Duration of Cardiac Antimicrobial Prophylaxis Outcomes Study

NCT05447559

Phase 4 Recruiting 9180 enrolled Monash University ANZCA CTN · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

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

Timeline

Start
2023-02-07
Primary completion
2027-12
Completion
2028-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Cefazolin Small molecule 2 g Intravenous

Indications

No indication recorded.