Evaluation of the Effect of Output on Skin Covered by a New Adhesive
Not Applicable
Completed
- Conditions
- Ileostomy - Stoma
- Interventions
- Other: New adhesive stripOther: 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
- Have given written informed consent
- Be at least 18 years of age and have full legal capacity
- Have had an ileostomy for more than one year
- Have intact skin on the area used in the evaluation
- Has an ileostomy with a diameter up to (≤) 35 mm
- Have a peristomal area accessible for application of patches/adhesive strips (assessed by investigating scientist) -
Exclusion Criteria
- Currently receiving or have within the past 2 month received radio- and/or chemotherapy
- Currently receiving or have within the past month received topical steroid treatment in the peristomal skin area or systemic steroid (tablet/injection) treatment.
- Are pregnant or breastfeeding
- Having dermatological problems in the peristomal- or abdominal area (assessed by investigating scientist)
- Participating in other interventional clinical investigations or have previously participated in this evaluation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Cohort 9 Standard adhesive strip This 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 9 New adhesive strip This 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
Name Time Method Trans epidermal water loss 6 hours The condition of the skin is measure by trans epidermal water loss after removing the adhesive strip.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Coloplast A/S
🇩🇰Humlebaek, Denmark