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Biomarker for acute wheezing exacerbation in preschool wheeze

Biomarker for acute wheezing exacerbation in preschool wheeze

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20200310002
Enrollment
120
Registered
2020-03-10
Start date
2019-02-14
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

5 years who had a diagnosis of asthma (include AD&#44
AR) by GINA guideline 2018 ,Children aged 2&#45
5 years recurrent wheezing ≥ 2 episodes confirmed by physician ,Healthy children aged 2&#45
5 years no underlying disease
Diagnostic,Diagnostic,Diagnostic
asthma group,Viral induced wheezing group,control group

Sponsors

research fund and deta analysis unit, Faculty of Medicine Ramathibodi Hospital
Lead Sponsor
research fund and deta analysis unit&#44
Collaborator
Faculty of Medicine Ramathibodi Hospital,research fund and deta analysis unit&#44
Collaborator
Faculty of Medicine Ramathibodi Hospital
Collaborator

Eligibility

Sex/Gender
All
Age
2 Years to 6 Years

Inclusion criteria

Inclusion criteria: asthma group : Children aged 2-5 years who had a diagnosis of asthma (include AD,AR) by GINA guideline 2018 Viral induced wheezing group :Children aged 2-5 years recurrent wheezing ≥ 2 episodes confirmed by physician control group :Healthy children aged 2-5 years no underlying disease

Exclusion criteria

Exclusion criteria: asthma group :Post respiratory tract infection in 4 week Coexisting disease : Malignancy Active autoimmune disease HIV infection Cardiovascular diseases Immunodeficiency Chronic lung disease -Inhaled corticosteroid use in 4 week Viral induced wheezing group :Post respiratory tract infection in 4 week Coexisting disease : Malignancy Active autoimmune disease HIV infection Cardiovascular diseases Immunodeficiency Chronic lung disease -Inhaled corticosteroid use in 4 week -allergen sensitization control group :Post respiratory tract infection in 4 week history allergen sensitization and atopy

Design outcomes

Primary

MeasureTime frame
serum periostin 1 year regression analysis

Secondary

MeasureTime frame
eosinophil cationic protein 1 year ANOVA

Countries

Thailand

Contacts

Public ContactPailin Yooma

Faculty of Medicine Ramathibodi Hospital,Mahidol Universit

bulin444@hotmail.com0896158466

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026