Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07475468

CP382 - Intermittent Catheter (IC) PRO Panel Plan

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Coloplast A/S · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

The registry's objective is to allow for insights into the needs of people with intimate healthcare needs from the user's perspective and experience. The registry will provide valuable information from the participants' perspective on several issues including, but not limited to product use and satisfaction, frequency of urinary tract infections, and quality-of-life related to IC use. The registry will allow for a more user-centric approach when listening and responding to the needs and challenges of IC users.

Conditions

Interventions

TypeNameDescription
OTHERNo Intervention: Observational CohortThere is only one observational cohort.

Timeline

Start date
2026-03-12
Primary completion
2032-09-30
Completion
2032-10-31
First posted
2026-03-16
Last updated
2026-03-16

Source: ClinicalTrials.gov record NCT07475468. Inclusion in this directory is not an endorsement.