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Идёт набор NCT07204561

CeraVe Effect on Restoring Skin Hydration as Maintenance Regimen in Subjects With Mild to Moderate Atopic Dermatitis

Без фазы С лечением Atopic Dermatitis (AD)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: CeraVe Moisturizing Cream, Galenico.
Кому может быть актуально
Состояния в реестре: Atopic Dermatitis (AD). Базовые параметры: 18 лет — 99 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Италия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Analysis of the CeraVe Emollient Effect on Restoring the Hydration of the Skin Barrier as Maintenance Regimen in Subjects With Mild to Moderate Atopic Dermatitis

Обзор

This is an open-label, randomised, comparative, prospective, interventional study of a cosmetic product.

Подробное описание

Atopic dermatitis is a common chronic inflammatory skin condition that affects individuals with specific alterations to the epidermal barrier. It is also characterised by defective ceramide production. Emollients play an important role in managing atopic dermatitis, including during the maintenance phase following topical cortisone therapy. However, the effect of CeraVe emollient cream on restoring skin barrier hydration has yet to be investigated.

The primary objective is to evaluate the effect of the CeraVe emollient on restoring skin barrier hydration as a maintenance regimen in subjects with mild to moderate atopic dermatitis. The secondary objectives are to evaluate and compare the cosmetic acceptability of CeraVe with that of a commonly used emollient produced in a licensed pharmacy laboratory, and to assess the differences in ADCT (Atopic Dermatitis Control Tool) scores between groups.

Subjects with mild-to-moderate atopic dermatitis (AD), as defined by an EASI score of 1-21, will be enrolled in the study. Only individuals with an EASI score reduction of at least 90% between screening (Day -15) and Visit 1 (Day 1) will be randomised into two groups. Group 1 will enter the maintenance phase with CeraVe emollient, while group 2 will be treated with a standard emollient. Both groups will be provided with a basic detergent for washing.

If the participant experiences a relapse of atopic dermatitis (AD), as reported in their diary and in the eCRF, they should discontinue the application of CeraVe Emollient or a common soft emollient. The subject should be examined by a physician and treated according to the severity of the AD. In this case, they will be withdrawn from the study.

Вмешательства

  • Другое CeraVe Moisturizing Cream
    During the 42-day maintenance phase, subjects must apply the CeraVe emollient twice a day after washing with the basic detergent as part of their normal hygiene routine.
  • Другое Galenico
    During the 42-day maintenance phase, subjects must apply the emollient twice a day after washing with the basic detergent as part of their normal hygiene routine.

Первичные конечные точки

  • Changes in EASI score [Срок оценки: From enrollment to the end of treatment at 6 weeks]
Вторичные конечные точки (4)
  • Cosmetic acceptability [Срок оценки: From visit 1 to the end of treatment at 6 weeks]
  • Changes in ADCT score [Срок оценки: From enrollment to the end of treatment at 6 weeks]
  • The number and proportion of subjects who experience a relapse of AD. [Срок оценки: From enrollment to the end of treatment at 6 weeks]
  • Changes in the visual appearance of the skin barrier over time, as observed by comparing images collected during the three scheduled study visits. [Срок оценки: From enrollment to the end of treatment at 6 weeks]

Критерии участия

Критерии включения

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.

Критерии исключения

  • 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).

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Италия · 1 центр
  • Fondazione PTV - Policlinico Tor Vergata — Roma

Идентификаторы

NCT: NCT07204561 · SID05

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗