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临床试验/NCT06300697
NCT06300697招募中不适用

Michigan Food and Atopic Dermatitis (M-FAD) Program - Molecular Analytics Project

University of Michigan1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年2月15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
200
试验地点
1
主要终点
Anaphylaxis occurrence rates in each group

研究概览

简要总结

This study will explore potential links between atopic dermatitis and food allergy. This information will be useful to determine atopic dermatitis and food allergy share unique biochemical or genetic identifiers useful for diagnosing and treatments in the future.

This is a mechanistic study consisting of obtaining blood and skin samples from participants at baseline. Individuals may also undergo a clinically indicated oral food challenge and have blood and skin samples collected at various times during the oral food challenge. This study will create a molecular map of the pathology of atopic dermatitis and food allergy. This information will be deployed to evaluate the hypothesis that atopic dermatitis and food allergy share unique genetic transcriptional signals in which the study team can then further analyze pathological pathways and cell types.

详细描述

This study will be funded by the National Institute of Health. Once the funds are received, the registration will be updated with this information.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
10 Years 至 55 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Food allergy-only group Inclusion Criteria:
  • •Have a known history of food anaphylaxis to peanut, tree nut, egg, milk, or sesame confirmed by an allergist.
  • •Have had skin and blood food allergy testing to the food allergen in question within the past 6 months. Meet the 80% likelihood positive predictive value threshold for allergy based on at least 1 of either the skin or blood immunoglobulin E (IgE) tests per current literature corrected for age. See protocol for more details.
  • •No history of atopic dermatitis
  • •Food allergy plus atopic dermatitis group Inclusion Criteria:
  • •- Meet the "food allergy only group" inclusion criteria except this group must also have atopic dermatitis.
  • •Atopic dermatitis without food allergy Inclusion Criteria:
  • •Have a present diagnosis of atopic dermatitis by an allergist and/or dermatologist.
  • •Have no history of food allergy, past or present.
  • •Control Group Inclusion Criteria:
  • •- No history of food allergy or atopic dermatitis, past or present.

排除标准

  • •for all groups:
  • •People younger than age 10 or older than age 55
  • •Any active cardiovascular disease, cancer, pulmonary disease except well-controlled asthma, or other condition that would preclude an OFC otherwise. Mild conditions that would not preclude an OFC are allowed (i.e., controlled hypertension or a surgically removed skin cancer that is resolved would not be exclusionary for this study, for example).
  • •Any medication use that cannot be stopped temporarily for the OFC that would interfere with the OFC result. Medications in this category include antihistamines (first or second generation) within 1 week.
  • •Any skin condition aside from atopic dermatitis per inclusion criteria groups that might impact the study, including such conditions as autoimmune skin conditions (such as psoriasis), congenital ichthyoses, hyper-IgE syndromes.
  • •Any recent change (within 6 months) of starting or stopping a biologic medication, such as dupilumab, tezepelumab, or others that might interfere with atopic dermatitis or food allergy.
  • •Any past or present history of oral immunotherapy (OIT) for any food allergen.
  • •Pregnancy - females of childbearing age will be asked and self-report pregnancy status.

研究组 & 干预措施

Control group Adult

Other

Participation will be approximately 14 days after enrollment.

干预措施: Data and biospecimen collection (Other)

Control group Adult

Other

Participation will be approximately 14 days after enrollment.

干预措施: Skin biopsies (Other)

Control group Adult

Other

Participation will be approximately 14 days after enrollment.

干预措施: Oral Food Challenge (OFC) procedures (Other)

Food allergy-only group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Data and biospecimen collection (Other)

Food allergy-only group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Skin biopsies (Other)

Food allergy-only group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Oral Food Challenge (OFC) procedures (Other)

Food allergy plus atopic dermatitis group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Data and biospecimen collection (Other)

Food allergy plus atopic dermatitis group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Skin biopsies (Other)

Food allergy plus atopic dermatitis group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Oral Food Challenge (OFC) procedures (Other)

Atopic dermatitis without food allergy group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Oral Food Challenge (OFC) procedures (Other)

Atopic dermatitis without food allergy group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Data and biospecimen collection (Other)

Atopic dermatitis without food allergy group

Other

Participation will be approximately 14 days after enrollment.

干预措施: Skin biopsies (Other)

Control Group less than 18 years old

Other

Participation will be approximately 14 days after enrollment.

干预措施: Data and biospecimen collection (Other)

Control Group less than 18 years old

Other

Participation will be approximately 14 days after enrollment.

干预措施: Oral Food Challenge (OFC) procedures (Other)

结局指标

主要结局

Anaphylaxis occurrence rates in each group

时间窗: Approximately 4 hours (Day 1 during the food challenge)

Anaphylaxis likelihood will be defined by the Brighton criteria. Any Brighton Level 1, 2, or 3 anaphylaxis. Score 1 = definite anaphylaxis, score 2 = probable anaphylaxis, score 3 = possible anaphylaxis.

次要结局

  • Anaphylaxis severity in each group(Approximately 4 hours (Day 1 during the food challenge))
  • Reaction rates in each group(Approximately 4 hours (Day 1 during the food challenge))
  • Anaphylaxis likelihood in each group based on the Brighton score(Approximately 4 hours (Day 1 during the food challenge))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Charles (Chase) Schuler

Assistant Professor of Internal Medicine and Assistant Professor of Mary H Weiser Food Allergy

University of Michigan

研究点 (1)

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