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Continence Care Registry

NCT04924569 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2026-05-08

No results posted yet for this study

Summary

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.

Conditions

  • Neurogenic Bladder
  • Non-Neurogenic Bladder

Sponsors & Collaborators

  • Parexel

    collaborator INDUSTRY

  • Hollister Incorporated

    lead INDUSTRY

Principal Investigators

  • Jessica Simmons, DNP, APRN, FNP-C, CWON, DNC · Hollister Incorporated

  • Diane Newman, D.N.P. F.A.A.N. B.C.B.-P.M.D. · University of Pennsylvania

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-24
Primary Completion
2030-05-31
Completion
2030-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04924569 on ClinicalTrials.gov