CP382 - Intermittent Catheter (IC) PRO Panel Plan
ConditionIntermittent Catheterization
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorColoplast A/S
About this trial
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.
Eligibility criteria
Qualifiers
Willing to give informed consent
18 years of age or above
Full legal capacity
Willing and able (self-assessed) to complete online questionnaires
Disqualifiers
None
Trial design
Treatments tested in this trial
- No Intervention: Observational Cohort
Treatment groups
No treatment groups listed
Locations
Sponsors and collaborators
Coloplast A/S
Lead sponsor
IQVIA Pty Ltd
Collaborator
Source ClinicalTrials.gov