Automated urIne Flow Detection to Reduce Errors and Nursing Workload

Completed

Conditions studied: Acute Kidney Injury, Kidney Injury

In brief

This study is an observational study which seeks to examine a) the accuracy of the Clarity Renal Monitoring System (Clarity RMS)® sensor kit at the bedside compared to manual urine output monitoring, b) total time/effort per patient with and without the device, c) the ease of use, clinical acceptance, and d) preliminary data on the detection of AKI using the Clarity RMS® sensor kit compared to standard care

Key facts

Study ID

NCT03636113

Run by

University of Pittsburgh

People needed

33

Starts

2018-07-11

Expected to finish

2021-01-31

Last updated by the study team

2021-05-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and Female ICU nurses
• Caring for 1 or more patients in ICU with a Foley catheter in situ

You may not qualify if…

• Nurse managing a patient who will be in ICU less than 4 hours
• Nurse managing a patient who is not producing urine

Where it is running

• UPMC Presbyterian Hosptial — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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