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Evaluation of Male and Female External Catheters for Urine Output Monitoring in the ICU

StatusEnrolling by Invitation
PhaseNot specified
SponsorC. R. Bard
Started
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Record History

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  1. Enrolling by invitation only
    • Start date changed from estimate of Aug 2026 to Sep 2, 2026
    • Eligibility criteria expanded, about 9 words
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
C. R. Bard
11 trials monitored
See 2 trials at risk
The goal of this observational pilot study is to learn about the ability of the PureWick® Flex Female External Catheter and the PureWIck® Male External Catheter to capture urine output in adult ICU patients compared to indwelling urinary catheters. The study will also gather feedback from ICU clinicians about the suitability of PureWick® urine output data to inform clinical decision-making.
Trial Details
NCT Number NCT07744945
Lead Sponsor C. R. Bard
Collaborators: Becton, Dickinson and Company
Conditions
(from sponsor)		 Urine Output, ICU Patients
Enrollment 32 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov