CP382 - Intermittent Catheter (IC) PRO Panel Plan

Starting soon

Conditions studied: Intermittent Catheterization

In brief

The aim is to create an electronic patient reported outcome (e-PRO) based registry, specifically for subjects using an intermittent catheter as their primary bladder emptying method.

Key facts

Study ID

NCT07475468

Run by

Coloplast A/S

People needed

1000

Starts

2026-06-01

Expected to finish

2032-10-31

Last updated by the study team

2026-05-13

Who can join

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

You may qualify if…

• Willing to give informed consent
• 18 years of age or above
• Full legal capacity
• Willing and able (self-assessed) to complete online questionnaires
• using intermittent catheterization as the primary method for bladder emptying

Full record on ClinicalTrials.gov

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