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临床试验/NCT05598762
NCT05598762尚未招募不适用

The Transcriptomic Study of Thai Patients With Atopic Dermatitis by Tape Strips

Queen Sirikit National Institute of Child Health1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年12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
尚未招募
入组人数
100
试验地点
1
主要终点
Immune biomarkers

研究概览

简要总结

This study will be use the tape strip technique to evaluate the skin biomarkers of atopic dermatitis among Thai patients to differentiate clinical phenotype.

详细描述

The patients will be enrolled in this study if they have been diagnosed with atopic dermatitis. All participants (AD patients and controls) will be evaluated their skin biomarkers by using tape stripping. The tape strips will be applied to the antecubital fossa to collect the epithelial samples. Then RNA was extracted from the tape strips for mRNA profiling to identify the immune and epidermal barrier genes.

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
1 Year 至 60 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Children (age 1-18 years old) with mild atopic dermatitis
  • •Children (age 1-18 years old) with moderate to severe atopic dermatitis
  • •Children (age 1-18 years old) with moderate to severe atopic dermatitis and food allergy
  • •Adult (age 18-60 years old) with atopic dermatitis
  • •Healthy individuals (1-60 years old)
  • •Patients with asthma (1-60 years old)

排除标准

  • •Active skin infections
  • •Used systemic immunosuppressants within 4 weeks
  • •Used topical steroids or immunomodulators within 1 week
  • •Used moisturizers within 12 hours before evaluation

研究组 & 干预措施

Children with mild atopic dermatitis

Active Comparator
  • age 1-8 years old
  • mild degree of atopic dermatitis

干预措施: Tape strips (Genetic)

Children with moderate-severe atopic dermatitis

Active Comparator
  • age 1-8 years old
  • moderate or severe degree of atopic dermatitis

干预措施: Tape strips (Genetic)

Children with food allergy and moderate-severe atopic dermatitis

Active Comparator
  • age 1-8 years old
  • moderate or severe degree of atopic dermatitis
  • IgE mediated food allergy

干预措施: Tape strips (Genetic)

Adult with atopic dermatitis

Active Comparator
  • age 18-60 years old
  • mild-severe atopic dermatitis

干预措施: Tape strips (Genetic)

Healthy

Active Comparator
  • age 1-60 years old
  • no history of atopic diseases

干预措施: Tape strips (Genetic)

Healthy with Asthma

Active Comparator
  • age 1-8 years old
  • doctor diagnosed asthma
  • no history of chronic or chronic relapsing eczema

干预措施: Tape strips (Genetic)

结局指标

主要结局

Immune biomarkers

时间窗: 1 month

Evaluated by RNA sequencing: RNA was extracted for real-time polymerase chain reaction (RT-PCR) with the miRNAeasy Mini Kit (Qiagen, Hilden, Germany). Reverse transcription to complementary DNA (cDNA) from RNA was carried out using the High Capacity cDNA reverse transcription (Thermo fisher). TaqMan Low Density Array (TLDA) cards (Thermo fisher) were used for quantitative reverse transcription polymerase chain reaction (qRT-PCR). 500pg total RNA was used for PreAMP pool. Eukaryotic 18S recombinant RNA (rRNA) was used as an endogenous control. Expression values were normalized to Rplp0

Cellular AD biomarkers

时间窗: 1 month

Evaluated by RNA sequencing: RNA was extracted for real-time polymerase chain reaction (RT-PCR) with the miRNAeasy Mini Kit (Qiagen, Hilden, Germany). Reverse transcription to complementary DNA (cDNA) from RNA was carried out using the High Capacity cDNA reverse transcription (Thermo fisher). TaqMan Low Density Array (TLDA) cards (Thermo fisher) were used for quantitative reverse transcription polymerase chain reaction (qRT-PCR). 500pg total RNA was used for PreAMP pool. Eukaryotic 18S recombinant RNA (rRNA) was used as an endogenous control. Expression values were normalized to Rplp0

Barrier biomarkers

时间窗: 1 month

chain reaction (RT-PCR) with the miRNAeasy Mini Kit (Qiagen, Hilden, Germany). Reverse transcription to complementary DNA (cDNA) from RNA was carried out using the High Capacity cDNA reverse transcription (Thermo fisher). TaqMan Low Density Array (TLDA) cards (Thermo fisher) were used for quantitative reverse transcription polymerase chain reaction (qRT-PCR). 500pg total RNA was used for PreAMP pool. Eukaryotic 18S recombinant RNA (rRNA) was used as an endogenous control. Expression values were normalized to Rplp0

次要结局

未报告次要终点

研究者

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

Tassalapa Daengsuwan

Assistant Professor

Queen Sirikit National Institute of Child Health

研究点 (1)

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