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NCT06714214
PREdiction of succeSSful weanING From Continuous Renal Replacement Theraphy: the Possible Role of Delta C-cistatin
Conditions: Acute Kidney Injury
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 152
Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna
Location: IRCCS Azienda Ospedaliero-Universitaria di Bologna - Anestesia polispecialistica e rianimazione Bologna Bologna
Summary
The goal of this observational study is to know if, in patients with acute kidney injury, naive for renal injurie, admitted to different ICUs, the change in plasma concentration of c-cistatin, between initiation and discontinuation of CRRT, is a predictive finding to optimize the withdrawal time of renal support
Eligibility Criteria
Inclusion Criteria:
* age ≥ 18 years;
* diagnosis of acute kidney injury (defined according to KDIGO 2012 criteria)
* need for support with CRRT according to the indications of the nephrologist consultants and Clinical Practice
* Obtaining informed consent
Exclusion Criteria:
* CRRT already ongoing (in another department not participating in the study) at the time of transfer/admission to intensive care;
* diagnosis of ESRF on admission;
* Discontinuation of CRRT under conditions that do not comply with the criteria established by the study;
* Need for CRRT not associated with AKI condition (e.g. elimination of toxicants);
* pregnant women;
* patient with known neoplastic disease.
Source: ClinicalTrials.gov (NCT06714214). StuddyBuddy aggregates publicly available trial information.