Comparative Study to Assess an Advanced Skin Protectant in the Management of Incontinence-associated Dermatitis

Inclusion Criteria: 1. Is the patient 18 years or older? 2. Has the patient or their legally authorized representative signed the Informed Consent Form? 3. Does the patient have IAD category 1A (IAD 1A: persistent redness without clinical signs of infection) or IAD category 2A (IAD 2A: skin loss without clinical signs of infection) in the study area (study area: the sacral region going down to the upper thighs, bordered approximately 5 cm below the gluteal fold? 4. Is the patient incontinent and does stool and/or urine come into direct contact with the skin? 5. Is the patient able to be turned/positioned with regard to skin assessment and photo documentation? 6. Is there a reasonable expectation that the patient will remain in the hospital setting for at least 7 days? Exclusion Criteria: 1. Is the patient pregnant or breast feeding? 2. Does the patient have a known hypersensitivity or allergy to acrylate or cyanoacrylate? 3. Does the patient have a stage II, III, IV or unstageable pressure ulcer or other suspected deep tissue injury in the study area? 4. Does the patient require topical treatment due to a fungal, bacterial or viral infection in the study area? 5. Does the patient require treatment with topical medication or product other than IAD treatment in the study area? 6. Does the patient have any other local dermatological disease or skin condition interfering with this study? 7. Does the patient have any medical condition (e.g. end of life, planned elective surgery) that in the opinion of the investigator should exclude him/her from participating in the study? 8. Does the patient participate in another study with a known or implied effect on skin barrier function?