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NOT YET RECRUITING
NCT07475468
CP382 - Intermittent Catheter (IC) PRO Panel Plan
Sponsor: Coloplast A/S
View on ClinicalTrials.gov
Summary
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 Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
1000
Start Date
2026-03-12
Completion Date
2032-10-31
Last Updated
2026-03-16
Healthy Volunteers
No
Conditions
Interventions
OTHER
No Intervention: Observational Cohort
There is only one observational cohort.