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The association between glucocorticoids on the neutrophil apopotsis and responsiveness to glucocorticoids in patients with asthma

The association between glucocorticoids on the neutrophil apopotsis and responsiveness to glucocorticoids in patients with asthma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-15007652
Enrollment
Unknown
Registered
2015-12-25
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

bronchial asthma

Interventions

steroid-sensitive asthma:oral glucocorticoid treatment
steroid-insensitive asthma:oral glucocorticoid treatment

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as asthma based on clinical symptoms and positive results of bronchial provocation or dilation tests according to the Global Initiative for Asthma (GINA) Guidelines; 2. Male or female aged 18 to 65 years with active asthma ,wheezing,shortness of breath, chest tightness or coughing, taking oral glucocorticoid treatment; 3. Agreed to join the study and signed a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of active lung diseases other than asthma (chronic obstructive pulmonarydisease, respiratorytract infections,bronchiectasis,etc); 2. Current and ex-smokers with more than 5 pack-years of smoking history; 3. Recently (within 4 weeks) treatment with systemic or inhaled corticosteroids; 4. Allergic to inhaled corticosteroids or beta 2 agonists; 5. Serious conditions such as heart, liver, kidneys, lungs, gastrointestinal tract, endocrine or blood system diseases. History of alcoholism and drug abuse; 6. Currently or recently participation in another clinical study; 7. Other reasons that the researchers believed inappropriate.

Design outcomes

Primary

MeasureTime frame
neutrophil apoptosis rate;improvement in FEV1 after treatment;

Secondary

MeasureTime frame
concentrations of inflammatory cytokines;

Countries

China

Contacts

Public ContactJungang Xie
xiejjgg@hotmail.com+86 027-83663617

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026