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Bandage showdown: which dressing keeps skin healthiest?

NCT ID NCT07547488

Knowledge-focused Sponsor: Essity Hygiene and Health AB Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study looks at how three different dressings change the pH of skin in simulated skin folds. Forty healthy adults will wear the dressings on their forearms for about 24 hours. Researchers will measure skin pH and hydration to see which dressing is gentlest on the skin.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Dressings (Sorbact® Ribbon, Sorbact® Compress, InterDry®)
What this could lead to
If successful, this could help choose dressings that keep skin healthier in folds, potentially reducing irritation and infections.
What could go wrong
This is a small, early study in healthy people, not patients. Results may not apply to real wounds or people with skin conditions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2025

Expected to finish

Apr 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Written informed consent to participate in this study 2. Healthy men and women between 18-80 years 3. Patient is mentally and physically able to participate in this study 4. Intact skin on the forearms without any signs of irritation 5. Agreed on not to shower or use cosmetic products on the arms the same day as visit 1 and during the study period 6. Agreed not to engage in intense physical activity throughout the study period Exclusion Criteria: 1. Skin disorder of any kind. 2. Known allergy to adhesives or/and any other component(silver) in the investigation devices. 3. Pregnant or lactating women. 4. Presence of tattoos on the forearms. 5. Ongoing medication with antibiotic. 6. Suffer from excessive sweating, hyperhidrosis.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Skin folds

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Essity Study site

    RECRUITING

    Mölndal, Sweden