Clinical Investigation Exploring a Newly Developed Ostomy Baseplate.

Inclusion Criteria: * Has given written informed consent * Is at least 18 years old * Has full legal capacity * Has an ileostomy with consistent liquid faecal output (6-7 Bristol scale). * Has used flat SenSura Mio 1-piece or 2-piece for at least 14 days before the inclusion. * Has had the stoma for at least 90 days * Has a stoma size less than 45mm in diameter * Has experienced symptoms of peristomal skin complications such as itching, burning, or pain in the peristomal area within the last 14 days * Has suitable peristomal skin area (assessed by investigator) to participate in investigation * Is willing to refrain from analgesics within 24 hours before the test days * Is willing to refrain from antihistamine within 96 hours before the test days * Is willing to refrain from steroid treatment within 24 hours before the test days Exclusion Criteria: * Is currently receiving or have within the past 60 days received radio-and/or chemotherapy. * low doses radio- and/or chemotherapy (assessed by Principal Investigator) is allowed for other indications than cancer. * Is currently receiving or have within the past 30 days received topical steroid treatment in the peristomal skin area, e.g., lotion or spray. * Is breastfeeding * Is pregnant based on urine pregnancy test. * Has known hypersensitivity towards any of the devices used in the investigation. * Participates in other clinical investigations. Exception: Participation in other Coloplast sponsored clinical investigations is …