MCO Membrane Efficiency in Septic Shock Patients

Status Completed

Clinical Trial Summary

This is a monocentre randomized pilot study. All patients received two consecutive RRT: CVVHD with MCO filter (Ultraflux® EMiC®2) and post-Continuous Veno-Venous Hemodiafiltration (CVVHDF) with HFF(AV1000S®) in a controlled randomized (1:1) blinded manner. Crossover randomized to sequence (A+B or B+A) for 48 h total without washout.

Clinical Trial Description

This is a monocentre randomized pilot study. All patients received CVVHD with MCO filter (Ultraflux® EMiC®2) and post-Continuous Veno-Venous Hemodiafiltration (CVVHDF) with HFF(AV1000S®) in a controlled randomized (1:1) blinded manner. Crossover randomized to sequence (A+B or B+A) for 48 h total without washout. The efficiency of the filters for small and middle molecules was compared in septic shock patients with AKI stage 3. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04834921
Study type	Interventional
Source	IRCCS Policlinico S. Matteo
Contact
Status	Completed
Phase	N/A
Start date	December 31, 2017
Completion date	January 31, 2021

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