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New Plant-Infused cream aims to heal Incontinence-Related skin damage

NCT ID NCT06370637

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a new barrier cream (Dermategrity Everyday Barrier Cream) that combines zinc oxide with a natural plant extract to heal skin damage caused by fecal incontinence. The cream is designed to protect the skin and block harmful enzymes from stool. Researchers will compare it to a standard zinc oxide cream in 40 adults over 14 days, measuring healing and symptom relief.

What this could mean

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

Active substance
Dermategrity Everyday Barrier Cream (zinc oxide plus plant extract)
What this could lead to
If it works, this cream could offer a more effective way to heal skin damage caused by fecal incontinence, improving comfort and quality of life.
What could go wrong
This is a small, early-stage trial with only 40 participants, so results may not apply to everyone. The cream is not a treatment for incontinence itself, and individual results may vary.

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.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Nov 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 * ≥18 years of age * Clinical diagnosis of incontinence-associated dermatitis resulting from diarrhea and/or fecal incontinence. * Able to provide written informed consent * Either able to self-administer barrier cream to the affected region OR administer with the assistance of a caregiver Exclusion Criteria * History of complex skin disorders (such as psoriasis or eczema) * Known allergy to any of the ingredients in the study product * Visual evidence of a bacterial skin infection * Use of a dressing or bandage covering the rash that cannot reasonably be removed for required study activities without compromising patient comfort or care. * Patients who are pregnant will not be excluded from the study unless they present with a rash or other skin conditions that may confound assessments * A medical condition that, in the opinion of the investigator, precludes the patient from being able to provide informed consent OR presents confounds which may bias the study outcomes

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Conditions

The condition(s) this trial relates to.

Fecal Incontinence

As listed by the trial registrant

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

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

  • University of Calgary Cumming School of Medicine

    Calgary, Alberta, T2N 2T8, Canada

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