ClinicalTrials.Veeva

Menu

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

F

FIZE Medical ltd

Status

Not yet enrolling

Conditions

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

Treatments

Device: FIZE kUO®

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

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.

Full description

The study involves adult patients undergoing coronary artery bypass graft (CABG) or valve replacement/repair surgeries. Utilizing the FIZE kUO® device, continuous urine output data will be collected to analyze responses to hemodynamic interventions, including fluid boluses and diuretics. Secondary objectives include assessing urine output differences in patients with and without postoperative acute kidney injury (AKI), responses to vasopressors, and capturing real-time urine output data from FIZE kUO® for observational analysis.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

45 participants in 1 patient group

Cardiothoracic ICU Patients
Description:
Adult patients (≥18 years old) undergoing coronary artery bypass graft (CABG) and/or valve surgery, admitted postoperatively to the Cardiothoracic Intensive Care Unit (CTICU), and connected to the FIZE kUO® device for real-time urine output monitoring as part of standard care.
Treatment:
Device: FIZE kUO®

Trial contacts and locations

1

Loading...

Central trial contact

Rinat Kalaora

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems