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Recruiting 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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06714214). StuddyBuddy aggregates publicly available trial information.