An Observational, Multinational, In Hospital Evaluation of Catheter Utilization Rates in Female Patients Using Indwelling Urinary Catheters and the PureWick™ Flex Female External Catheter Across Europe and the Middle East
← catalyst calendarNCT07798128 · readout in 301 d
Sponsored by Becton, Dickinson and Company (industry) · BDX — their whole pipeline →.
Phase
—
Status
Not yet recruiting
Study type
Observational
Enrollment
240estimated
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-09-01
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-11-06 | estimated | When the study began enrolling |
| Primary completion | 2027-06-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-08-31 | estimated | The whole study's end, after follow-up |
| First posted | 2026-09-01 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-09-01 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Urinary Incontinence
- Limited Mobility
Interventions
- Device: PureWick™ Flex Female External Catheter (FFEC)
- Device: Indwelling Urinary Catheter (IUC)
Primary outcome
what the primary-completion date above is the date OFIndwelling Urinary Catheter (IUC) Utilization Rate
measured From enrollment (informed consent) until hospital discharge or up to 40 days, whichever occurs first
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