Eczema blood test could reveal hidden immune clues
NCT ID NCT05868824
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at blood inflammation in people with moderate to severe atopic dermatitis (eczema). Researchers will take blood samples before and after 3 months of treatment to see how immune signals change. The goal is to better understand the immune response in different patient groups. Only 11 participants are enrolled, so this is a small, early-stage observation.
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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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11 people
The number who actually took part.
- Started
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Jun 2023
- Expected to finish
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Mar 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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18 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient aged ≥ 18 years. * Patient with clinically diagnosed atopic dermatitis according to the criteria of Hanifin and Rajka. * Moderate to severe defined by an Investigator's Global Assessment ³3 and eligible to systemic treatment. * If the subject is a woman of childbearing potential, she has a negative urine pregnancy test. * Subject is non-pregnant, non-lactating and is not planning for pregnancy during the study period. * Subject is in good general health and free of any known disease state or physical condition which, in the investigator's opinion, might impair his/her evaluation or which exposes the subject to an unacceptable risk by study participation. * Subject is able to comprehend and willing to sign an Informed Consent and/or Assent Form. * Affiliation to a social security scheme. * Signed informed consent Exclusion Criteria: * Vulnerable person: pregnant or nursing woman, minor, adult under guardianship or deprived of liberty * Patient with an infection * Patient with other systemic inflammatory disease * Patient with anti-inflammatory or immunosuppressive therapy * Patient with a contraindication to JAK inhibitors * Participants in other clinical therapeutic studies involving a drug that may interfere with the present evaluation
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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
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Nice University Hospital
Nice, France, 06200, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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