Could a seawater balm soothe eczema as well as the gold standard?
NCT ID NCT07358000
First seen Jun 24, 2026 · Last updated Sep 09, 2026 · Updated 2 times
Summary
This study compares a new emollient balm made from seawater (Relipid+) to a leading balm (Lipikar) for mild to moderate eczema in people aged 6 months to 70 years. The goal is to see if the new balm works just as well at reducing symptoms and improving skin health. Researchers will also check if it helps the skin's microbiome.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Relipid+ balm (Active Oligo Skin from seawater)
- What this could lead to
- If it works, this could offer a more affordable, effective emollient option for managing eczema symptoms.
- What could go wrong
- This is a small, early-stage trial (86 people) comparing two balms, not a cure. The new balm may not be as effective as the standard one.
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
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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
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About 86 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: Patients aged 6 months to 70 years with mild to moderate atopic dermatitis (SCORAD \< 40) Time to treatment initiation \< 72 hours between initial assessment and balm application Affiliated with the French national health insurance system and French-speaking Written informed consent must be obtained Exclusion Criteria: Patients who decline participation Patients under legal guardianship, curatorship, legal protection, or judicial safeguard Patients with a SCORAD indicating the need for systemic therapy
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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CHU Caen Normandie
RECRUITINGCaen, Normandy, France
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