Not Yet RecruitingNot Applicable

Assessment of Wound Care Product Skin Adhesion

Sweden48 participantsStarted 2025-09

Plain-language summary

The purpose of this exploratory study is to assess the adhesive forces to skin of samples over the period of 24 hours to establish the peel-off measurement method at the Essity study site.

Who can participate

Age range18 Years – 70 Years

SexALL

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Inclusion criteria

✓. Written informed consent to participate in the study.
✓. Willingness to actively participate in the study and to come to the scheduled visits.
✓. Female and/or male.
✓. From 18 to 70 years of age.
✓. Minimal hairiness on the back (the test area)

Exclusion criteria

✕. Female participants: Pregnancy or lactation.
✕. Drug or alcohol addiction.
✕. AIDS, HIV-positive or infectious hepatitis.
✕. Conditions which exclude a participation or might influence the test reaction/evaluation.
✕. Participation or being in the waiting period after participation in cosmetic and/or pharmaceutical studies pertaining to the test area.
✕. Cancer not being diagnosed as cured and requiring chemotherapy, irradiation and/or hormonal treatment within the last 2 years.
✕. Diabetes mellitus (type 1 and 2).
✕. One of the following illnesses with reduced physical capability/fitness: asthma (symptom-free allergic asthma is not an exclusion criterion), hypertension, cardiovascular diseases.

What they're measuring

Adhesion

Timeframe: After 24 hours of tape use

Adhesive forces measured in N/cm

Timeframe: 1-2 months

Trial details

NCT IDNCT07136870

SponsorEssity Hygiene and Health AB

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-10

Contact for this trial

Shabira Abbas Senior Scientist

+46 0766486586 Sabira.Abbas@essity.com

View on ClinicalTrials.gov More Skin (FLACC Scores of Test Subjects) After Tape Removal trials