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ClinicalTrials.gov record
Completed Not applicable Interventional

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

ClinicalTrials.gov ID: NCT07282860

Public ClinicalTrials.gov record NCT07282860. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 11:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Controlled Crossover Study on the Safety, Efficacy, and Patient Reported Outcome Measures Comparing the PureWick™ System With an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT07282860
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
C. R. Bard
Industry
Enrollment
120 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 20, 2025
Primary completion
Jun 21, 2026
Completion
Jun 21, 2026
Last update posted
Aug 3, 2026

2025 – 2026

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Lakeview Clinical Research, LLC Guntersville Alabama 35976
Novak Clinical Research Tucson Arizona 85741
American Institute of Research Los Angeles California 90017
Finlay Medical Research Greenacres City Florida 33467
Finlay Medical Research Miami Florida 33126
Sonar Clinical Research Atlanta Georgia 30315
Eagle Clinical Research Chicago Illinois 60621
Vida Clinical Studies Dearborn Heights Michigan 48127
Trialfinity Clinical Research Center Hamilton New Jersey 08619
Inno MDR Clinical Hamilton New Jersey 08690
Albuquerque Clinical Trials Albuquerque New Mexico 87102
Prime Global Research The Bronx New York 10456
Monroe Biomedical Research North Charleston South Carolina 29406
Trio Clinical Trials Houston Texas 77008
R&H Clinical Research Katy Texas 77494

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07282860, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 3, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07282860 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →