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The Influence of Output on Skin Covered by Adhesive With Topfilm

Not Applicable
Completed
Conditions
Ileostomy - Stoma
Interventions
Other: New adhesive strip
Other: Standard adhesive strip
Registration Number
NCT03044275
Lead Sponsor
Coloplast A/S
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
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 -

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Cohort 8Standard adhesive stripThis is a sub-study testing the effect of real output on the skin applied under two adhesive strips. New adhesive strip Standard adhesive strip
Cohort 8New adhesive stripThis is a sub-study testing the effect of real output on the skin applied under two adhesive strips. New adhesive strip Standard adhesive strip
Primary Outcome Measures
NameTimeMethod
Trans epidermal water loss6 hours

the condition of the skin (trans epidermal water loss) is measured after removing the adhesive from the skin

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Coloplast A/S

🇩🇰

Humlebaek, Denmark

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