Who is eligible for clinical trial NCT04924569?

Participants must meet protocol criteria for Neurogenic Bladder. Confirm exact inclusion and exclusion requirements with the study coordinator.

Does clinical trial NCT04924569 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2026-05-04

Continence Care Registry (NCT04924569)

🔵 Active, Not Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: Hollister Incorporated

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (7 items) and avoid the listed exclusions (4 items).

Location: Hollister Incorporated — Libertyville, Illinois

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Is at least 18 years of age; male or female.
Is performing transurethral intermittent catheterization.
Uses intermittent catheter(s) from any manufacturer as a form of management for urinary retention or incomplete bladder emptying.
Must be able to provide informed consent and have no cognitive impairment that would hinder the ability to provide informed consent or self-reported data.
Lives and has permanent residence in one of the countries that the study is being conducted at time of enrollment (USA, Canada, UK, Germany, France, The Netherlands, or Italy)
Is willing and able to complete electronic questionnaires monthly for the first year of data collection and quarterly thereafter or appoint a caregiver proxy.
Is able to read and respond to the questionnaires in the language options provided for a given country (e.g. French Canadian or English for Canada)

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
Performs non transurethral catheterization, e.g., stoma.
Participating in a clinical study involving transurethral intermittent self-catheterization at the time of enrollment.
Employee of Sponsor at the time of enrollment.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

Hollister Incorporated — Libertyville, Illinois

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

🏛️ View Official NIH Record ↗