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Clinical Trial Summary

The goal of this assessor blinded randomized controlled trial is to compare a lock solution containing taurolidine, citrate and heparin to a heparin only lock solution for the prevention of central line associated bloodstream infections in paediatric oncology patients with a central venous access device.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05740150
Study type Interventional
Source Princess Maxima Center for Pediatric Oncology
Contact Ceder H van den Bosch, MSc
Phone +31625395632
Email c.h.vandenbosch-4@prinsesmaximacentrum.nl
Status Recruiting
Phase N/A
Start date October 27, 2020
Completion date December 1, 2023

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