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CompletedNCT02210169

RCT of Continuous Versus Intermittent Infusion of Vancomycin in Neonates

A Randomised Controlled Trial (RCT) of Continuous and Intermittent Infusion of Vancomycin in Neonates

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
111 (actual)
Sponsor
Murdoch Childrens Research Institute · Academic / Other
Sex
All
Age
90 Days
Healthy volunteers
Not accepted

Summary

Babies aged 0 to 90 days with a suspected infection requiring treatment with vancomycin will be recruited. They will be randomised to receive vancomycin as an intermittent infusion (over 1 hour) or as a continuous infusion (over 24 hours). The hypothesis is that administering vancomycin as a continuous infusion will result in improved attainment of target concentrations in blood at steady state (when the drug is in equilibrium) compared to intermittent infusion.

Conditions

Interventions

TypeNameDescription
DRUGContinuous infusion of vancomycinContinuous infusion of vancomycin will be given as a loading dose over 1 hour then as a continuous infusion over a 24-hours period.

Timeline

Start date
2014-09-01
Primary completion
2018-04-01
Completion
2018-05-01
First posted
2014-08-06
Last updated
2018-11-02

Locations

2 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT02210169. Inclusion in this directory is not an endorsement.

RCT of Continuous Versus Intermittent Infusion of Vancomycin in Neonates (NCT02210169) · Clinical Trials Directory