CHU Caen Normandie
Caen, Normandy, France
NCT Number: NCT07358000
The therapeutic cornerstone for mild to moderate forms of atopic dermatitis (AD) relies on the combination of topical corticosteroids and emollients. However, the daily application of emollients can be burdensome, leading to poor adherence, treatment fatigue, and therapeutic failure, often prompting a switch in emollient products.
Emollients therefore represent a true therapeutic challenge. They also raise economic concerns, as they are not reimbursed by national health insurance, unlike topical corticosteroids. This results in an out-of-pocket expense for patients, adding a significant financial burden in the context of this chronic skin condition.
Laboratoires Gilbert have developed and patented an active ingredient derived from seawater (Active Oligo Skin), formulated and produced at their pharmaceutical site in Hérouville Saint Clair. This active compound has shown promising in vitro and preclinical results in modulating inflammatory mechanisms involved in sensitive and atopic skin.
The objective of this clinical trial is to compare the efficacy of Laboratoires Gilbert's patented emollient balm (Relipid+) with a reference emollient balm considered the "gold standard" and most frequently prescribed on the market (Lipikar Baume AP+M, La Roche-Posay) for atopic dermatitis. The hypothesis is that the test balm will be at least as effective as the gold standard (non-inferiority) in clinical terms, with an added benefit on microbiome diversity-an emerging and critical issue in the management of atopic dermatitis.
Trial opening soon.
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Interventional
Not applicable
Caen, Normandy, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Application of daily emollient
Time frame: Day 0; Day 7; Day 28; Day 70
SCORAD (Scoring Atopic Dermatitis) : from 0 up to 103
Time frame: Day 7 and Day 14
DLQI questionnaire, scoring to 0 up to 30
Time frame: Day 4 and Day 14
Itch Numeric Rating Scale from 0 to 10
Time frame: Day 70 at the end of the study
Amount of topical steroids used
University Hospital, Caen
Other
AIMSI Trial : Double-blind, Randomized, Non-inferiority Trial in Atopic Dermatitis: Comparison of Lipikar Balm and Relipid+ Balm in the Treatment of Mild to Moderate Atopic Dermatitis in Children and Adults
Acronym: AIMSI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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