PREdiction of succeSSful weanING From Continuous Renal Replacement Theraphy: the Possible Role of Delta C-cistatin
- Conditions
- Acute Kidney Injury
- Registration Number
- NCT06714214
- Brief 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
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 152
- 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
- CRRT already ongoing (in another department not participating in the study) at the time of transfer/admission to intensive care;
- need for RRT (any type and modality) in the 14 days prior to enrolment;
- diagnosis of AKD/CKD/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;
- presence of known thyreopathy
- Continuous use of corticosteroids
- patient with known neoplastic disease.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the change in plasma concentration of c-cistatin between initiation and discontinuation of CRRT is a predictive finding in patients with acute kidney injury admitted to the ICU From enrlollment to the weaning from CRRT and 14 days after To verify whether the change in plasma concentration of c-cistatin between initiation and discontinuation of CRRT is a predictive finding in patients with acute kidney injury admitted to the ICU It is measured as (cistatin at weaning minus cistatin basal) divided by cistatine basal, in percentage
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (2)
IRCCS Azienda Ospedaliero-Universitaria di Bologna - Anestesia e Terapia Intensiva nelle emergenze locali, regionali e nazionale e nella chirurgia addominale maggiore
🇮🇹Bologna, Italy
IRCCS Azienda Ospedaliero-Universitaria di Bologna -Anestesiologia e terapia intensiva polivalente
🇮🇹Bologna, Italy