CP384 - Ostomy Care (OC) PRO Panel Plan

NCT07589907 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-05-15

No results posted yet for this study

Summary

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).

Conditions

  • Ostomy
  • Ileostomy - Stoma
  • Urostomy

Sponsors & Collaborators

  • IQVIA Pty Ltd

    collaborator INDUSTRY
  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Ann-Sophie Luel-Brockdorff, PhD · Coloplast A/S

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-01
Primary Completion
2032-09-30
Completion
2032-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07589907 on ClinicalTrials.gov