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临床试验/NCT07228962
NCT07228962招募中不适用

Using a Non-invasive Micro-suction Biomarker Extraction Device to Understand Atopic Eczema in Babies

King's College London1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年3月31日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Inflammatory Cytokine levels in ISF

研究概览

简要总结

This project aims to establish whether an adapted extraction device is tolerable and will be able to measure chemical signals in baby's ISF. Insight into the chemical profiles found in the skin interstitial fluid (ISF) of healthy and diseased babies will identify signals that can be used to investigate the causes of eczema and propose new preventative strategies and effective treatments.

Specifically, it aims to:

  1. Demonstrate that the developed ISF device can be used to extract biomarkers from the skin of babies non-invasively and is tolerable (not causing significant discomfort, bruising, or blister formation).
  2. Compare the profile of chemical markers present in the ISF of healthy babies with babies that have developed eczema.
  3. Compare the biomarker levels extracted from babies with eczema in lesional and non-lesional skin using the developed ISF device.
  4. Compare the microbiome and metabolome profiles from swabs taken from babies with healthy skin and with eczema in lesional and non-lesional skin (exploratory outcome).

详细描述

Eczema is a skin condition that affects up to 20% of children worldwide, and its numbers are increasing. Our goal is to learn more about eczema by studying how immune signals in the skin differ between babies with eczema and those with healthy skin. To do this, investigators will gently use a non-invasive device to extract a tiny amount of fluid from the top layer of baby's skin(Interstitial Skin Fluid). By studying these samples, investigators want to compare the immune signals of healthy skin and skin affected by eczema. This research aims to deepen our understanding of why eczema causes inflammation and to identify the specific signals involved in this process, particularly in babies.

A total of 30 babies will be recruited, of which 15 will be healthy and 15 have eczema. They will be invited to attend for one visit lasting 1-1.5 hours. During the study visit, clinical information such as demographics, medical history and co-morbidities as well as eczema treatments (where applicable) and other skin care practices will be collected. For babies that have eczema, an eczema area and severity index (EASI) assessment will be conducted. For all participants enrolled onto the study, Interstitial Skin Fluid (ISF) samples will be extracted from the skin using a painless, non-invasive device that is well-tolerated and will not cause any pain or skin damage to the baby. Samples for assessing the skin microbiome will be collected, including skin swabs and tape strips taken in a pain-free manner. Skin barrier function assessments such as Transepidermal water loss (TEWL) will also be performed helping us understand how well the baby's skin holds onto moisture. This is a painless and non-invasive device that doesn't cause any discomfort to the baby.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
0 Months 至 6 Months(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy babies and babies with atopic dermatitis up to 6 months old.
  • •Ability of parents/guardians/caregivers to provide written informed consent for study participation.
  • •Willingness of parents/guardians/caregivers to comply with all study requirements.
  • •Parents/guardians/caregivers competent use of English language.

排除标准

  • •Parents/guardians/caregivers unable to give informed consent.
  • •Preterm birth (defined as birth before 37 completed weeks gestation).
  • •Significant inflammatory skin disease at birth.
  • •Baby has any other serious health issue.

研究组 & 干预措施

Healthy babies

Babies up to 6 months old without eczema

Babies with Eczema

Babies up to 6 months old with eczema

结局指标

主要结局

Inflammatory Cytokine levels in ISF

时间窗: At enrolment

The ISF extraction device will be applied to the baby's calf for a total of 5 min (both lesioned and non-lesioned skin in eczema presenting babies) and an ISF sample will be collected using an extraction gauze. The amount of protein or sodium will be used to determine the volume of ISF sampled. In addition, the release of soluble mediators such as IL-10 and TGF-beta as well as other Th1/Th2 cytokines IFN-Ɣ IL-1β IL-2 IL-4 IL-5 IL-13 IL-6 IL-8 (CXCL8) IL-10, IL-33, IL-12p70, TNF-α, GM-CSF, TSLP will be measured using an MSD cytokine analyser.

次要结局

  • TEWL(At enrolment)
  • Microbiome profiles and Metabolite levels(At enrolment)
  • Tolerability of the use of the ISF Device(At enrolment)
  • Investigator Assessments(At enrolment)
  • TEWL(At enrolment)
  • Tolerability of the use of the ISF Device(At enrolment)
  • Investigator Assessments(At enrolment)
  • Microbiome profiles and Metabolite levels(At enrolment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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