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NCT06666426 · ClinicalTrials.gov registry record · NA
This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.
A NA study, sponsored by C. R. Bard.
- Completed
- Registry status
- NA
- Development phase
- 171
- Enrollment target
NCT06666426: Completed NA study, sponsored by C. R. Bard.
NCT06666426 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 171 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06666426, a NA study, has completed, sponsored by C. R. Bard.
- COMPLETED
- Registry status
- NA
- Development phase
- 171 participants
- Enrollment target
Study Summary
This post-market study will assess the performance of and user experience with the PureWick™ System in a home setting. The study will also observe safety of the study device and collect information from participants about their quality of life before and after using the device.
Primary Outcome
Daily capture rate (captured as % of urine captured by device and collected in canister, measured by weight)
Interventions
- DEVICE PureWick System
- DEVICE Hollister Female Urinary Pouch External Collection Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 171 participants |
| Start Date | 2024-10-31 |
| Est. Completion | 2025-06-30 |
| Phase | NA |
What the finished NCT06666426 record still lists
NCT06666426 is an interventional study that assigns participants to a tested intervention. The registered 171 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 2 interventions - of which PureWick System is the first listed.
NCT06666426 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06666426 about?
NCT06666426 is a clinical study titled "This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.". This post-market study will assess the performance of and user experience with the PureWick™ System in a home setting. The study will also observe safety of the study device and collect information from participants about their quality of life before and after using the device.
What is the current status of trial NCT06666426?
This trial is currently completed. It is a NA study. The enrollment target is 171 participants. The study started on 2024-10-31. Estimated completion is 2025-06-30.
What interventions are being tested in trial NCT06666426?
The interventions under investigation include: PureWick System (DEVICE), Hollister Female Urinary Pouch External Collection Device (DEVICE).
Who is sponsoring clinical trial NCT06666426?
This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06666426's enrollment target sits among peer trials
171 612th of 2000 higher than 1,387 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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