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NCT06850259 · ClinicalTrials.gov registry record · NA
This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.
A NA study, sponsored by C. R. Bard.
- Completed
- Registry status
- NA
- Development phase
- 15
- Enrollment target
NCT06850259 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 15 participants.
The verdict
NCT06850259, a NA study, has completed, sponsored by C. R. Bard.
- COMPLETED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
Study 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.
Interventions
- DEVICE PureWick™ System
- DEVICE UltraFlex™ Self-Adhering Male External Catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2025-03-21 |
| Est. Completion | 2025-06-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06850259
The ClinicalTrials.gov registry entry for NCT06850259 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is C. R. Bard, which has 75 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which PureWick™ System is the first listed.
NCT06850259 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06850259 about?
NCT06850259 is a clinical study titled "This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.". 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.
What is the current status of trial NCT06850259?
This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2025-03-21. Estimated completion is 2025-06-15.
What interventions are being tested in trial NCT06850259?
The interventions under investigation include: PureWick™ System (DEVICE), UltraFlex™ Self-Adhering Male External Catheter (DEVICE).
Who is sponsoring clinical trial NCT06850259?
This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.
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