Phase
Condition
Low Blood Sodium (Hyponatremia)
Renal Failure
Vascular Diseases
Treatment
Restrictive UFnet Rate Strategy
Liberal UFnet Rate Strategy
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 18 years or older
Stage 3 acute kidney injury according to the Kidney Disease: Improving GlobalOutcomes (KDIGO) criteria
Started or intending to start CKRT for volume management
Attending intensivist or nephrologist intending to remove net fluid using CKRT forat least 48 hours
Exclusion
Exclusion Criteria:
Respiratory distress due to pulmonary edema or fluid overload in unintubatedpatients
Massive volume infusion (i.e., >200 mL/h for >6 hours of continuous infusion)
No intention to remove net fluid as determined by attending intensivist ornephrologist
Attending intensivist or nephrologist believes that the protocol will not befollowed
Continuous net fluid removal for >48 hours prior to study enrollment
Patients on chronic outpatient hemodialysis
Patients with history of, or current admission for kidney transplantation
Patients on comfort measures only orders.
Moribund not expected to survive >24 hours
Confirmed pregnancy
Patients treated with extracorporeal membrane oxygenation, ventricular assistdevice, or intra-aortic balloon pump
Organ donors with neurological determination of death (i.e., brain dead donors)
Drug overdose requiring CKRT for drug clearance
Enrollment in a concurrent interventional clinical trial with direct impact on fluidbalance (e.g., >500 mL study drug administration)
Study Design
Study Description
Connect with a study center
Mayo Clinic
Rochester, Minnesota 55905
United StatesSite Not Available
Mayo Clinic
Rochester 5043473, Minnesota 5037779 55905
United StatesSite Not Available
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania 15261
United StatesSite Not Available
University of Pittsburgh Medical Center
Pittsburgh 5206379, Pennsylvania 6254927 15261
United StatesSite Not Available

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