CP384 - Ostomy Care (OC) PRO Panel Plan
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 living with a stoma (ileostomy, colostomy or urostomy).
Eligibility criteria
Qualifiers
18 years of age or above
full legal capacity
willing and able to complete online questionnaires
have either an ileostomy, a colostomy, or a urostomy
Disqualifiers
Cannot have a scheduled stoma reversal surgery
Cannot have more than one stoma
Trial design
Treatments tested in this trial
- Not listed
Trial groups
1,000 Participants
are grouped into 1 trial groupLocations
Sponsors and collaborators
Coloplast A/S
Lead sponsor
IQVIA Pty Ltd
Collaborator
Source ClinicalTrials.gov