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Study identifier: NCT05770622 Synced from ClinicalTrials.gov · July 28, 2026
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Improving Therapeutic Drug Monitoring and Dosing for Vancomycin in Young Infants With Infections (VANCAPP) (Part 2)

Condition: Sepsis · Infections · Bacteremia  ·  Sponsor: Murdoch Childrens Research Institute

PhasePhase 4
Planned participants40
Who can joinAll sexes, 0 Days to 90 Days
Healthy volunteersNo

About this study

A challenge to intermittent vancomycin dosing in young infants is the avoidable delay caused by the need to wait until steady state (i.e. when the drug concentrations are in equilibrium) to measure a vancomycin concentration, as this generally occurs 24 to 48 hours after starting treatment. If the target concentration is not achieved, the dose needs to be adjusted, resulting in further delays in an infant achieving the concentration required to treat their infection. The purpose of this study is to assess the use of early therapeutic drug monitoring (first-dose trough) and, if needed, early dose adjustment, in achieving target vancomycin concentrations at steady state. A dose adjustment calculator (available through a web application) will be used to determine the need for dose adjustment (based on predicted steady state concentration) and recommend an adjusted dose if required.

This description comes directly from the study's public registry record.

Talk to the study team

Amanda Wilkins, MBBS  ·  9345 5522  ·  amanda.wilkins@rch.org.au

Amanda Gwee, MBBS  ·  9345 5522  ·  amanda.gwee@rch.org.au

Always discuss trial participation with your own doctor first.

Locations (4)

Royal Children's Hospital MelbourneMelbourne, Victoria, AustraliaRecruiting
Monash NewbornMelbourne, AustraliaNot Yet Recruiting
Royal Hospital for WomenSydney, AustraliaNot Yet Recruiting
The Children's Hospital at WestmeadSydney, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT05770622