Assessement of the Peal Force Needed to Peel New Adhesives From the Skin

N/ACompletedNCT03289013

Coloplast A/S5 enrolled

Overview

This study investigates the adhesion of new adhesives to the skin.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Ileostomy - Stoma

Interventions

Standard adhesive 1OTHER

This strip consists of a standard hydrocolloid adhesive found in ostomy devices

Standard adhesive 2OTHER

This strip consists of a standard hydrocolloid adhesive found in ostomy devices

LT-2OTHER

Newly developed adhesive

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

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 intact skin on the area used in the investigation Exclusion Criteria: 1. Currently receiving or have within the past 2 months received radio- and/or chemotherapy 2. Currently receiving or have within the past months received topical steroid treatment in the abdominal skin area or systemic steroid (tablet/injection) treatment. 3. Are pregnant or breastfeeding 4. Have dermatological problems in the abdominal area (assessed by investigator)

Locations (1)

Coloplast A/S

Humlebæk, Denmark

Outcomes

Primary Outcomes

Swelling of the adhesive

1\. Swelling of adhesive strips measured by weight (Difference between weight of strip before and after test)

Time frame: 21 days

Data from ClinicalTrials.gov

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