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Study identifier: NCT07282860 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males

Condition: Urinary Incontinence  ·  Sponsor: C. R. Bard

PhaseNA
Planned participants120
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (15)

Lakeview Clinical Research, LLCGuntersville, Alabama, United States
Novak Clinical ResearchTucson, Arizona, United States
American Institute of ResearchLos Angeles, California, United States
Finlay Medical ResearchGreenacres City, Florida, United States
Finlay Medical ResearchMiami, Florida, United States
Sonar Clinical ResearchAtlanta, Georgia, United States
Eagle Clinical ResearchChicago, Illinois, United States
Vida Clinical StudiesDearborn Heights, Michigan, United States
Trialfinity Clinical Research CenterHamilton, New Jersey, United States
Inno MDR ClinicalHamilton, New Jersey, United States
Albuquerque Clinical TrialsAlbuquerque, New Mexico, United States
Prime Global ResearchThe Bronx, New York, United States

+ 3 more locations — full list on the registry record.

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