MedPath

Evaluation of the Effect of Output on Skin Covered by a New Adhesive

Not Applicable
Completed
Conditions
Ileostomy - Stoma
Interventions
Other: New adhesive strip
Other: Standard adhesive strip
Registration Number
NCT03044288
Lead Sponsor
Coloplast A/S
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6
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 9Standard adhesive stripThis is a sub-study testing the effect of real output applied under two adhesive strips on the skin. Standard adhesive strip and a strip with a newly developed adhesive (new adhesive strip)
Cohort 9New adhesive stripThis is a sub-study testing the effect of real output applied under two adhesive strips on the skin. Standard adhesive strip and a strip with a newly developed adhesive (new adhesive strip)
Primary Outcome Measures
NameTimeMethod
Trans epidermal water loss6 hours

The condition of the skin is measure by trans epidermal water loss after removing the adhesive strip.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Coloplast A/S

🇩🇰

Humlebaek, Denmark

© Copyright 2025. All Rights Reserved by MedPath