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Clinical Trial Summary

Impact of the hemoadsorption with Cytosorb on hemodynamic in pediatric patients with septic shock: a prospectic pediatric pilot study


Clinical Trial Description

Prospective interventional pilot study included children with septic shock, weight ≥ 10 Kgs and requiring continuous kidney replacement therapy. Cytosorb (CytoSorbents Inc, New Jersey, USA) cartridge was added to CKRT every 24 hours for a maximum of 96 hours. A control group of matched patients was also identified from an external database. The primary outcome of the study was the proportion of patients who achieved an equal or more than 50% relative reduction in vasopressors or inotropes dose from baseline to the end of treatment. Secondary outcomes included doses of vasopressors and inotropes, hemodynamic and biological changes, changes in severity scores and 28-day mortality. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05658588
Study type Interventional
Source Ospedale Pediatrico Bambin Gesù
Contact
Status Completed
Phase N/A
Start date September 1, 2019
Completion date October 1, 2021

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