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ACTIVE NOT RECRUITING
NCT03715179

Observational Study of Ostomy Consumers

Sponsor: Hollister Incorporated

View on ClinicalTrials.gov

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