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Automated urIne Flow Detection to Reduce Errors and Nursing Workload

NCT03636113 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2021-05-10

No results posted yet for this study

Summary

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

Conditions

Interventions

DEVICE

Clarity RMS Electronic Sensor

The urinary foley catheter with electronic sensor will be placed within the Operating Room prior to surgery. Upon arrival to the ICU, the device will be connected to an electronic console by study coordinator. The study coordinator will weigh the urine drainage bag and record the weight every hour for 4-6 hours. The device will record urine flow on a 15 minute interval up to 6 hours

Sponsors & Collaborators

  • RenalSense Ltd

    collaborator UNKNOWN

  • University of Pittsburgh

    lead OTHER

Principal Investigators

  • John Kellum, MD · University of Pittsburgh

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-11
Primary Completion
2018-12-28
Completion
2021-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03636113 on ClinicalTrials.gov