Phase
Condition
Kidney Disease
Kidney Failure
Soft Tissue Infections
Treatment
Commercial membrane for Extracorporeal Blood Purification Therapy (EBPT)
Clinical Study ID
All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: patients who meet all the following inclusion criteria may be included in this study:
Admission to ICU
Indications for at least one of the following extracorporeal blood purificationtreatments:
Continuous Renal Replacement Therapy (CRRT) / Intermittent Hemodialysis (IHD) /Hybrid therapies for renal support/replacement;
Immunomodulation therapy in critically ill patients using hemodiafilters withlarger pore sizes characterized by enhanced transmembrane clearance of largermolecules (such as cytokines), hemodiafilters with enhanced unselectiveabsorption of cytokines and/or endotoxins, cartridges with enhanced absorptionof cytokines and/or endotoxins, techniques aimed at improving extracorporealremoval of cytokines and/or endotoxins.
It should be underlined that the lack of established guidelines on the use of membranes for extracorporeal blood purification (and on RRTs in general) leads to variability in clinical practice and treatments are initiated in accordance with the judgement of the responsible physician. Under these circumstances, it is preferable to keep inclusion criteria as wide as possible so as to obtain a real picture of clinical practice worldwide.
Exclusion
Exclusion Criteria: besides contraindications to the use of the EBP adopted (as from the manual of instructions), there are no exclusion criteria.
Study Design
Study Description
Connect with a study center
Azienda Ospedaliero Universitaria Careggi
Florence, 50100
ItalyActive - Recruiting
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