Actively Recruiting

Age: 3Years - 14Years
All Genders
Healthy Volunteers
ID06840717

Association Between Cytokines Gene Single Nucleotide Polymorphisms and Type 2 Inflammatory Asthma in Children

Led by Guangzhou Institute of Respiratory Disease · Updated on 2025-02-21

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how genetic differences called single nucleotide polymorphisms (SNPs) affect children with type 2 inflammation-related asthma. This observational study compares children diagnosed with asthma who show signs of type 2 inflammation to healthy children. The goal is to better understand how these genetic variations influence asthma development and to support personalized treatment and prevention strategies. The study includes two groups: children with asthma who meet specific inflammation criteria and healthy children. Researchers measure several type 2 inflammation markers, such as the fraction of exhaled nitric oxide, blood eosinophil counts, sputum eosinophil percentages, and serum immunoglobulin E levels. They also assess lung function through tests like forced expiratory volume in one second (FEV1), forced vital capacity (FVC), FEV1/FVC ratio, and peak expiratory flow (PEF). Genetic testing for SNPs is performed to explore differences between groups. Participants will be evaluated during outpatient visits, where lung function tests and inflammation marker measurements will be collected. The main outcomes include type 2 inflammation indicators, pulmonary function measures, and genetic polymorphism data. This process helps researchers identify risk factors and differences in asthma linked to genetics, with the study lasting until December 2025.

CONDITIONS

Brief Title

Association Between Genetic Polymorphisms and Type 2 Asthma in Children

Who Can Participate

Age: 3Years - 14Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children diagnosed with asthma according to the 2023 GINA guidelines
  • No other diseases causing wheezing and cough like acute laryngitis, diphtheria, congenital airway abnormalities, or tracheal foreign bodies
  • No use of antibiotics or systemic hormone medications in the 2 weeks before hospital visit
  • No other complications such as congenital heart disease, pneumonia, gastroesophageal reflux disease, or muscle dysplasia
Not Eligible

You will not qualify if you...

  • Children who have taken immunosuppressants, antibiotics, or similar drugs for a long time before admission
  • Children with primary immunodeficiency disease
  • Children and families who do not cooperate or refuse to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo assessments including type 2 inflammation indicators, pulmonary function tests, and genetic testing for single nucleotide polymorphisms.

1 outpatient visit

Long-term Monitoring

Duration - Up to 2 years

Participants are observed to compare genetic polymorphisms and inflammatory markers between children with type 2 asthma and healthy controls.

No scheduled visits; observational follow-up

Trial Site Locations

Total: 1 location

1

Guangzhou institute of respiratory disease

Guangzhou, Guangdong, China, 510120

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Research Team

L

Lihong Sun, M.D.

L

Lanying Cheng

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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