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Observational Study of Ostomy Consumers
Sponsor: Hollister Incorporated
Summary
The purpose of this longitudinal prospective observational study is to collect electronic Patient Reported Outcome (ePRO) data over a 7-year period directly from people living with an ostomy and their caregivers (participants were re-consented with version 3 of the Protocol in 2020 which indicated a study duration of 5 years, and version 6 of the Protocol in 2025 extending for an additional 2 years). Research participants will be asked to self-report on the ostomy pouching systems they typically use and other various aspects of living with an ostomy and/or caring for an individual living with an ostomy.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
5000
Start Date
2018-10-04
Completion Date
2027-02
Last Updated
2026-02-03
Healthy Volunteers
No
Conditions
Locations (1)
Hollister Incorporated
Libertyville, Illinois, United States