Continence Care Registry

Running, not enrolling

Conditions studied: Neurogenic Bladder, Non-Neurogenic Bladder

In brief

This observational research study aims to build a multinational electronic patient-reported outcomes (ePRO) registry of adult end users in outpatient and community settings using intermittent catheter(s) to void via the urethra to manage urinary retention and incomplete bladder emptying. Research participants will be asked to self-report on various attributes of their currently prescribed intermittent catheters and other various aspects of using an intermittent catheter.

Key facts

Study ID
NCT04924569
Run by
Hollister Incorporated
People needed
600
Starts
2021-05-24
Expected to finish
2030-05-01
Last updated by the study team
2026-05-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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