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Clinical Trial

This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.

NCT: NCT06850259 · COMPLETED

NCT IDNCT06850259
StatusCOMPLETED
Start Date2025-03-21
Completion2025-06-15
SponsorC. R. Bard (INDUSTRY)
First posted
Last updated

Brief Summary

This post-market study will assess the performance of and user satisfaction with the PureWick® Male External Catheter in a home setting. The study will also observe safety of the study device and collect information from participants about their experience using the device.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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