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CBD cream shows promise for eczema itch relief in small study

NCT ID NCT07301658

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 1 time

Summary

This 56-day study tested a cream containing CBD and cherimoya fruit extract on 42 children and adults with mild-to-moderate atopic dermatitis (eczema). Participants applied the cream twice daily. Researchers measured skin redness, dryness, itching, and sleep quality. The goal was to see if the cream could improve skin barrier function and comfort.

What this could mean

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

Active substance
cream containing cannabidiol (CBD) and Annona cherimola fruit extract
What this could lead to
If it works, this could offer a gentle, non-drug option to ease itching and dryness for people with mild-to-moderate atopic dermatitis.
What could go wrong
This was a small, completed study with no control group, so results may not be definitive. The cream is a cosmetic product, not a medicine, so benefits may be modest.

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

42 people

The number who actually took part.

Started

Feb 2023

Finished

Aug 2024

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * Sex: both. * Age: from 0 months onwards (includes children and adults). * Atopic-prone skin. * Mild to moderate flare-up. * Skin dryness. * Signed informed consent (by the volunteer or legal guardian as applicable). * Adequate understanding of the clinical study by the participant or legal guardian. * Good physical and psychological health. * No application of any product on the experimental area on the first day of the trial. * Availability to guarantee visits to the research center. Exclusion Criteria: * History of allergies to cosmetic products. * Recent surgery or treatments in the study area. * Oncology patients. * Use of antihistamines and antibiotics within 15 days prior to the start of the study. * Treatment with antihistamines, antibiotics, corticosteroids, immunosuppressants or completion of such treatment within 15 days prior to the start of the study. * Use of any other product for dermatitis during the study. * Sun exposure or UVA rays during the study. * Participation in another clinical study. * Health problems that may compromise adherence to the study protocol.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • i+Med S.Coop.

    Vitoria-Gasteiz, Álava, 01510, Spain

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