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

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.

NCT Number	NCT07744945
Lead Sponsor	C. R. Bard Collaborators: Becton, Dickinson and Company
Conditions	Urine Output, ICU Patients
Enrollment	32 participants
Start Date	2026-08
Primary Completion	2026-10 (estimated)
Study Completion	2026-10 (estimated)
Updated on ClinicalTrials.gov	2026-08-04