Observational Study of Ostomy Consumers — OSO  

Ostomy Clinical Trial

Official title: Observational Study of Ostomy Consumers

Status Recruiting

Clinical Trial Summary

The purpose of this longitudinal prospective observational study is to collect electronic Patient Reported Outcome (ePRO) data over a 5-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). 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.

Clinical Trial Description

This longitudinal prospective observational study is designed as an ePRO registry to collect data from consumers with an ostomy (ileostomy, colostomy, or urostomy) in the United States, Canada, and United Kingdom. An ePRO registry provides a relevant data source founded on the patient's voice. As such, an ePRO registry will be invaluable for prospective observational research aiming to investigate associations of ostomy pouching systems (inclusive of accessories) with peristomal skin health, participant QoL, caregiver burden, product satisfaction, and Healthcare Resource Utilization (HRU). Information from this registry will inform and guide industry healthcare providers and payers in decision-making and subsequent research that factors in the patient and caregiver perspectives. The current study does not test any specific a priori hypotheses. ;

Related Conditions & MeSH terms

• Ostomy

• NCT number: NCT03715179
• Study type: Observational [Patient Registry]
• Source: Hollister Incorporated
• Contact: Manager Global Clinical Affairs
• Phone: +18479321845
• Email: mackenzie.juckett@hollister.com
• Status: Recruiting
• Start date: October 4, 2018
• Completion date: February 2025