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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02504528
Other study ID # GIRD201534
Secondary ID BAPT201534
Status Completed
Phase N/A
First received July 8, 2015
Last updated February 14, 2018
Start date July 1, 2015
Est. completion date February 1, 2018

Study information

Verified date February 2018
Source Guangzhou Institute of Respiratory Disease
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to establish the methodology of bronchial provocation tests with house dust mites in China, and to evaluate its safety and effects on upper and lower airways inflammation.


Description:

After screening,each participant undergo baseline lung function test,airway inflammation evaluation (blood and sputum eosinophils count,interleukin-13 (IL-13),FeNO)and airway responsiveness tests(methacholine bronchial provocation,nasal histamine provocation).

On the second day,the participant undergo bronchial house dust mites challenge tests.

On the third day,the participant undergo the lung function test,airway inflammation evaluation (blood and sputum eosinophils count,IL-13,FeNO)and airway responsiveness tests(methacholine bronchial provocation,nasal histamine provocation).


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 1, 2018
Est. primary completion date July 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of asthma;

- Sensitive to house dust mite;

- Stable for more than 4 weeks with FEV1=70%pred

Exclusion Criteria:

- exacerbation within 3 months;

- upper airway infections within 6 weeks;

- concomitant of hypertension or heart diseases;

- pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
house dust mites
house dust mites(two-fold increasing concentration of house dust mite (HDM) extract, dilutions prepared starting from 1:8, 1:16, 1:32, 1:64, 1:128, 1: 256, 1:512, 1:1024,……)

Locations

Country Name City State
China Guangzhou institute of respiratory disease Guangzhou Guangdong

Sponsors (2)

Lead Sponsor Collaborator
Guangzhou Institute of Respiratory Disease Firestone Institute for Respiratory Health

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other correlate of IL-4,IL-13,periostin with provocative concentration induced a 20% decrease in FEV1 to house dust mite in asthmatic By Comparison with methacholine provocation test 30 mins and 24 hours after house dust mites bronchial challenge
Other Incidence and Severity of Adverse Events During The House Dust Mite Bronchial Provocation Test By Comparison with methacholine provocation test at 30 min and 24 hours after challenge test. 30 minutes, 7 hours and 24 hours after house dust mites bronchial provocation
Primary percentages of the participants that tested positive to house dust mites bronchial provocation 30 minutes after house dust mites bronchial provocation
Secondary Changes of the percentages of eosinophils in sputum, nasal lavage and fractional exhaled nitric oxide (FeNO) from baseline 30mins, 7 and 24 hours after bronchial challenge
Secondary Changes of provocative concentration induced a 20% decrease in forced expiratory volume at one second (FEV1) to methacholine before and after house dust mites bronchial provocation 24 hours after house dust mites bronchial challenge
Secondary percentages of the participants that tested positive to house dust mites bronchial provocation measured by impulse oscillometry 10 minutes after house dust mites bronchial provocation
Secondary Changes of provocative concentration induced a 60% increase in nasal airway resistance to histamine before and after house dust mites bronchial provocation By Comparison with methacholine provocation test 24 hours after house dust mites bronchial challenge
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