Evaluation of a Novel Electronic Urine Output Monitor (eUOM)

Completed

Conditions studied: Oliguria, Polyuria

In brief

Urine output and urine drain line pressure were monitored while urine was drained into either: 1. Accuryn Urine Output Monitor (Potrero Medical) OR 2. Criticore Monitor (Bard Medical)

Key facts

Study ID

NCT02195713

Run by

Potrero Medical

People needed

20

Starts

2014-07-01

Expected to finish

2015-02-01

Last updated by the study team

2016-02-22

Who can join

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

You may qualify if…

• Patient must ≥ 18 years of age
• Patient has a Foley catheter and urine collection system is in place per standard clinical decision
• Estimated length of placement of the Foley is 48 hours minimum
• Burn injury ≥ 20% and ≤ 80% total body surface area (TBSA)
• Subject or subject's legally authorized representative is able to give informed consent before entering the study

You may not qualify if…

• Currently pregnant or breastfeeding
• Clinical signs or symptoms of a urinary tract infection (UTI)
• Clinical signs or symptoms of a vaginal infection
• Currently has bladder or urethral trauma
• Use of investigational drug/device therapy within the past 4 weeks

Where it is running

• Joseph M. Still Burn Center at Doctors Hospital — Augusta, Georgia, United States
• The University of Texas Medical Branch (UTMBP) — Galveston, Texas, United States

Full record on ClinicalTrials.gov

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