Urine Output Monitoring to Guide Fluid and Diuretic Therapy in Cardiac ICU Patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this prospective observational study, researchers collect real-time urine output from patients in the cardiothoracic ICU who have undergone CABG or valve surgery and are monitored with the FIZE kUO device. They examine how urine output responds to fluid boluses, diuretics, and other hemodynamic interventions, with a focus on informing fluid management. Secondary analyses compare outcomes between patients who do and do not develop postoperative AKI and evaluate responses to vasopressors. Data from continuous urine monitoring are analyzed to identify patterns associated with improved or worsened renal perfusion after surgery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Adults aged 18 years and older scheduled for CABG or valve surgery and expected postoperative admission to CTICU
2. Ability to provide informed consent

Exclusion Criteria:

1. Pregnancy
2. Preoperative dialysis (chronic or acute)
3. Enrollment in other interventional trials assessing urine output or AKI

Where it's running

• Rabin Medical Center
  Petah Tikva, Israel Recruiting

Study contacts

• Study coordinator: Rinat Kalaora
• Email: rinat.kalaora@fizemedcial.com
• Phone: +972-544-750887

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.