Ileostomy - Stoma
Conditions
Brief summary
The study investigates the impact real output has on adhesion of new adhesives
Interventions
Sponsors
Coloplast A/S
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Have given written informed consent * Be at least 18 years of age and have full legal capacity * Have had a stoma for more than one year * Have intact skin on the area used in the evaluation * Has a stoma 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 peri-stomal- or abdominal area (assessed by investigating scientist) * Actively participating in other interventional clinical investigations or have previously participated in this investigation.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Trans epidermal water loss | 8 hours | The trans epidermal water loss is measured on the peristomal skin using a probe. The trans epidermal water loss is a measure for the skins barrier function. There is always a loss of water from the skin due to natural evaporation. However, when the skin barrier is damaged the evaporation will increase leading to an increase in the trans epidermal water loss.Thus, trans epidermal water loss is used to assess the damage to the skin. Maesurents are taken at time 0 and after 8 hours of output exposure to the skin. |
Countries
Denmark
Outcome results
None listed