Coloplast A/S
Humlebæk, 3050, Denmark
NCT Number: NCT03044275
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.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Humlebæk, 3050, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This is a newly developed adhesive strip that in the future might be part of an ostomy device
This is a standard adhesive strip (hydrocolloid). The adhesive is a part of an ostomy device
Time frame: 6 hours
the condition of the skin (trans epidermal water loss) is measured after removing the adhesive from the skin
Coloplast A/S
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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