CeraVe Effect on Restoring Skin Hydration as Maintenance Regimen in Subjects With Mild to Moderate Atopic Dermatitis
Recruiting now · Not applicable
Conditions studied: Atopic Dermatitis (AD)
In brief
This is an open-label, randomised, comparative, prospective, interventional study of a cosmetic product.
Key facts
- Study ID
- NCT07204561
- Run by
- Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse
- People needed
- 98
- Starts
- 2025-03-25
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2025-10-02
Who can join
Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects with clinically confirmed mild-to-moderate atopic dermatitis (AD), as defined by an Eczema Area and Severity Index (EASI) score of 1-21, whose lesions will clear after treatment with a steroid and who will experience at least a 90% reduction in their EASI score.
- Participants of any gender, aged 18 years or over, from any phototype or ethnic group.
- Participants must be willing and able to give informed consent to participate in the study.
You may not qualify if…
- Age <18 years. Participants who are unwilling or unable to give informed consent to participate in the study.
- Receiving any systemic treatment for atopic dermatitis (AD), including corticosteroids, cyclosporine, any approved biologics or JAK inhibitors.
- Any dermatological disorder which, in the investigator's opinion, may interfere with the accurate evaluation of the subject's skin characteristics (except AD).
Where it is running
- Fondazione PTV - Policlinico Tor Vergata — Roma, RM, Italy (enrolling)
Full record on ClinicalTrials.gov
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