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Clinical Trial Summary

The adequacy of the currently used dosing regimen of glycopeptides (vancomycin and teicoplanin) and beta-lactam antibiotics (amoxicillin-clavulanic acid, piperacillin-tazobactam, ceftazidim) in patients with end-stage kidney disease receiving intermittent hemodialysis is studied by evaluating pharmacokinetics-pharmacodynamics (PK-PD) target attainment. A population pharmacokinetic study is performed to assist the selection of the optimal individualized dose for patients undergoing intermittent dialysis, taking into consideration as many relevant variables as possible.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03909698
Study type Observational
Source University Hospital, Ghent
Contact
Status Completed
Phase
Start date September 15, 2016
Completion date March 31, 2022

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