Principal Investigator: Myer, Brian S., MD
Study Sponsor: Fistula Solution
Location: HealthPartners Specialty Center
Phase of Study: Pivotal Trial
Purpose of study: The purpose of the study is to determine if a new ostomy pouch wound management device, called the Limpet, prevents complications and improves the quality of life for people living with an ostomy and/or fistula compared to the current pouch devices used.
Inclusion Criteria:
– 18 years of age or older
– Undergone ileostomy surgery, have a pre-existing ileostomy with skin damage or have a fistula
Additional inclusion/exclusion criteria apply. Please contact the study team for more information.
Exclusion Criteria:
– Scheduling/planning chemotherapy or other radiation treatment
– Pregnant
– Unable/unwilling to attend follow-up appointments
Additional inclusion/exclusion criteria apply. Please contact the study team for more information.
Study Contact:
Allison Kehren
(651) 254-5342
allison.j.kehren@healthpartners.com
