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Clinical Trial Summary

Recently, it was reported that when vancomycin levels are determined after port sampling, levels can be falsely increased potentially leading to wrong dose adjustments.

The investigators conducted an in vitro experiment using several central venous port devices, in which different flushing techniques were evaluated yielding residual vancomycin levels of less than 0.5 mg/L.

In this study, the investigators want to evaluate this flushing technique in vivo in 15 patients admitted with catheter-related infection and treated with systemic vancomycin and vancomycin antibiotic lock.

The purpose is to assess if correct flushing can avoid spurious vancomycin levels obtained via port sampling.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01661361
Study type Observational
Source Universitaire Ziekenhuizen Leuven
Contact Isabel Spriet, PharmD PhD
Phone 0032 16 34 30 80
Email isabel.spriet@uzleuven.be
Status Not yet recruiting
Phase N/A
Start date September 2012
Completion date December 2012

See also
  Status Clinical Trial Phase
Terminated NCT00633061 - Identification and Treatment of Clinically Silent Catheter-Related Deep Vein Thrombosis in Children With Cancer Phase 2