Preliminary Study of Peel Force and Discomfort of Removal of Adhesive Barriers in Normal and Peristomal Skin

Inclusion Criteria: * Colostomy, Ileostomy, or Urostomy patients at least 6 months post-surgery * Males or females, age 18 to 80 years old at the time of enrollment * Body Mass Index (BMI) between 18 and 50 * Willing to have two approximately 5" x 5" areas of the abdomen trimmed with a surgical clipper -- one in a ring around the stoma, and one on the opposite side * Willing to remain within the testing room for the duration of the study * Willing to allow a third person in the room as a witness for the duration of the study * Able to position oneself onto and off of the examining table without the assistance of the Investigator * Willing to refrain from vigorous exercise for the duration of the study * Willing to not take any anti-inflammatory medications (except for Tylenol/acetaminophen) starting 48 hours prior to the study and for the duration of the study * Willing to bring an extra barrier and replace their barrier worn during the study. * Willing to follow the protocol as demonstrated by signing the Informed Consent Form * In the opinion of the Investigator or qualified site personnel is qualified to participate Exclusion Criteria: * Clinically significant diseases, which may or may not be confined to the testing site, that may contraindicate participation; including but not limited to psoriasis, eczema, atopic dermatitis, and active cancer * Use of topical drugs on the application site within 1 month. * Use of lotions, creams, powders or oils on the application site in the 24 hours prior to application * Pregnancy, lactation or planning a pregnancy as determined by interview only * Other medical conditions, for example uncontrolled diabetes, which in the Investigator's judgment, makes the subject ineligible or places the subject at undue risk * Participation in any clinical test either using the abdomen as a test site or using systemic therapy within the previous thirty days * Damaged skin or other skin conditions in or near test sites which includes sunburn, scars, numerous moles or other disfiguration of the test site * Significant adipose tissue at the test site that would preclude adequate adhesion of the study devices * Known allergy to any of the test materials