Urine Output Response to Fluid and Diuretic Therapy in Cardiac ICU Patients Monitored With FIZE kUO®

ConditionsAKI - Acute Kidney Injury Cardiac Surgery Fluid Therapy Hemodynamic Instability Postoperative Complications

Trial statusNot yet recruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age18+

SponsorFIZE Medical ltd

About this trial

This prospective observational study evaluates the real-time urine output response to fluid therapy and diuretics in cardiothoracic intensive care unit (CTICU) patients monitored with the FIZE kUO® device. The study aims to assess how continuous urine output monitoring can inform fluid management and improve patient outcomes post-cardiac surgery.

Eligibility criteria

Qualifiers

Adults aged 18 years and older scheduled for CABG or valve surgery and expected postoperative admission to CTICU

Ability to provide informed consent

Disqualifiers

Pregnancy

Preoperative dialysis (chronic or acute)

Enrollment in other interventional trials assessing urine output or AKI

Trial design

Treatments tested in this trial

FIZE kUO®

Treatment groups

45 Participants

are divided into 1 treatment group

Sponsors and collaborators

FIZE Medical ltd

Lead sponsor

Source ClinicalTrials.gov