Evaluation of the Influence of Output on Skin Covered by Newly Developed Adhesives

Coloplast A/S4 enrolled

Overview

The study investigates the impact real output has on peristomal skin covered by a newly developed adhesive and a standard adhesive.

Study Type

INTERVENTIONAL

Allocation

Purpose

BASIC_SCIENCE

Masking

NONE

Enrollment

Conditions

Ileostomy - Stoma

Interventions

Standard adhesive stripOTHER

This is a standard adhesive strip (hydrocolloid)

New adhesive stripOTHER

This a newly developed adhesive strip.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Have given written informed consent 2. Be at least 18 years of age and have full legal capacity 3. Have had an ileostomy for more than one year 4. Have intact skin on the area used in the evaluation 5. Has an ileostomy with a diameter up to (≤) 35 mm 6. Have a peristomal area accessible for application of patches/adhesive strips (assessed by investigating scientist) Exclusion Criteria: 1. Currently receiving or have within the past 2 month received radio- and/or chemotherapy 2. Currently receiving or have within the past month received topical steroid treatment in the peristomal skin area or systemic steroid (tablet/injection) treatment. 3. Are pregnant or breastfeeding 4. Having dermatological problems in the peristomal- or abdominal area (assessed by investigating scientist) 5. Participating in other interventional clinical investigations or have previously participated in this evaluation

Locations (1)

Coloplast A/S

Humlebæk, Denmark

Outcomes

Primary Outcomes

Trans epidermal water loss

The condition of the skin (transepidermal water loss) is measured after removing the adhesive by TE

Time frame: 4-24 hours

Data from ClinicalTrials.gov

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