The purpose of this study is to estimate the incidence and severity of peristomal skin lesions and evaluate the progression of the peristomal skin condition at 8-15 days following application of the barrier.
Study Type
OBSERVATIONAL
Enrollment
2,000
Independent Nurse Consultant
Tucson, Arizona, United States
John Muir Health Concord Campus
Concord, California, United States
Conn. Clinical Nursing Associate, LLC
Plymoth, Connecticut, United States
Peristomal skin condition
Change in peristomal skin condition from baseline as assessed with the SACS Instrument
Time frame: At day 12
Peristomal skin condition
Change in peristomal skin condition from baseline as assessed with the SACS instrument
Time frame: at 1 month
Level of satisfaction
Subjects satisfaction as measured with a satisfaction survey
Time frame: At 2 months
Accessory usage
Subjects use of additional products in stoma care.
Time frame: Up to 2 months
Peristomal Skin Condition
Change in peristomal skin condition from baseline as assessed with the SACS instrument
Time frame: At 2 months
Level of satisfaction
Subjects level of satisfaction as measured by a satisfaction survey
Time frame: At 12 days
Level of satisfaction
Subjects level of satisfaction as measured with a satisfaction survey
Time frame: At 1 month
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