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临床试验/NCT07358000
NCT07358000招募中不适用

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

University Hospital, Caen1 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
86
试验地点
1
主要终点
SCORAD measurment

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Care Provider)

入排标准

性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Patients who decline participation
  • Patients under legal guardianship, curatorship, legal protection, or judicial safeguard
  • Patients with a SCORAD indicating the need for systemic therapy

研究组 & 干预措施

Bras Lipikar AP+M (La Roche Posay)

Active Comparator

干预措施: Baume Relipid+ (Other)

Bras baume RELIPID+ (Laboratoires Gilbert)

Experimental

干预措施: Baume Relipid+ (Other)

结局指标

主要结局

SCORAD measurment

时间窗: Day 0; Day 7; Day 28; Day 70

SCORAD (Scoring Atopic Dermatitis) : from 0 up to 103

次要结局

  • DLQI (Quality of life)(Day 7 and Day 14)
  • Itch NRS scale (Itch Numeric Rating Scale)(Day 4 and Day 14)
  • Use of topical steroids(Day 70 at the end of the study)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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