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Recruiting NCT07022314

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

Conditions: AKI - Acute Kidney Injury, Cardiac Surgery, Fluid Therapy, Hemodynamic Instability, Postoperative Complications

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 45
Sponsor: FIZE Medical ltd

Location: Rabin Medical Center Petah Tikva

Summary

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

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

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

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07022314). StuddyBuddy aggregates publicly available trial information.