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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.
Keep your clinical trial research organized — questions to ask, what to expect, and key details.
Ann-Sophie luel-Brockdorff, Sr. Clinical Strategy Project Manager, PhD
CONTACT
+45 49112078dkasib@coloplast.comLead Sponsor
Coloplast A/S
Collaborators
NCT06529107 · Intermittent Catheterization, Conversion of Evidence
NCT06429631 · Neurogenic Bladder, Spinal Cord Injury, and more
Use Clareo to keep notes, questions, trial details, and next steps organized before and after appointments.
Start free trial →Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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