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Asthma Biomarkers for Predicting Response to Therapy

Novel Asthma Biomarkers to Predict the Response to Inhaled Corticosteroid

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01973751
Enrollment
148
Registered
2013-10-31
Start date
2013-11-30
Completion date
2016-07-31
Last updated
2016-05-16

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

Conditions

Asthma

Brief summary

Novel asthma biomarkers to predict the response to inhaled corticosteroid Brief description: This will be a single center study of asthmatic subjects and healthy controls which will investigate mechanisms underlying different response to inhaled corticosteroid, the mainstay of asthma therapy. Only about half of the asthmatic patients have improved lung function after treatment of inhaled corticosteroid. The investigators hypothesize that there are biomarkers such as epithelial cytokines (IL-25, IL-33, TSLP) in airway tissues or plasma of asthmatic patients which could predict the response of asthmatic patients to inhaled corticosteroid. Finding novel asthma biomarker will help the clinicians to choose the optimal treatment for individual asthmatic patient.

Interventions

DRUGBudesonide

Inhaled powder of inhaled corticosteroid, 2 puffs (200mcg) twice a day for 8 weeks

Sponsors

Tongji Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

Group A: Inclusion Criteria: * Male and female subjects between the ages of 18 and 70 years * No respiratory symptoms * Normal spirometric value and methacholine PD20 \>2.5mg Group B: Inclusion Criteria: * Male and female subjects between the ages of 18 and 70 years * History of asthma * No use of oral or inhaled corticosteroids for the treatment of asthma * No use of leukotriene antagonist for the treatment of asthma * Hyperreactivity to methacholine (PD20 FEV1 Methacholine \< 2.5 mg) and/or ≥12% increase in FEV1 following inhalation of 200μg salbutamol * Asthma symptoms of episodic cough, wheeze and/or breathlessness

Exclusion criteria

* Current or former smokers * Pregnant women * Subjects with a history of lung disease other than asthma * Subjects with a history of a medical disease, which in the opinion of the investigator may put the subject at extra risk from study-related procedures or because the disease may influence the results of the study

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline airway epithelial cytokines expression, FEV1 and methacholine PD20 at 4 and 8 weeks8 weeks1. The baseline expression of airway epithelial cytokines (IL-25, IL-33, TSLP) and/or Th2 cytokines (IL-4, IL-5, IL-13) in bronchial brushing, bronchial biopsy and peripheral blood in healthy control subjects and asthmatic patients. 2. Change of forced expiratory volume of the 1st second (FEV1) and accumulated dosage of methacholine provoking a 20% fall of in forced expiratory volume in the first second (FEV1 PD20) of asthmatic patients after treatment with inhaled budesonide or non-intervention for 4 and 8 weeks.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026