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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02591550
Other study ID # coughlongli
Secondary ID
Status Recruiting
Phase N/A
First received October 21, 2015
Last updated October 28, 2015
Start date March 2015
Est. completion date December 2017

Study information

Verified date October 2015
Source The First Affiliated Hospital of Guangzhou Medical University
Contact Kefang Lai, PhD
Phone 8620-83062893
Email klai@163.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The aim of this study is described as follows,

1. To establish a validated method to test cough reflex sensitivity conducted by transient receptor potential vanilloid 1(TRPV1).

2. To observe the variance of cough reflex sensitivity conducted by transient receptor potential ankyrin 1(TRPA1) of chronic patients and the relationship between cough reflex sensitivity conducted by TRPA1 and conducted by TRPV1.

3. To study the distribution of TRPA1 and TRPV1 channels and their relationship to cough reflex sensitivity.


Description:

This study is divided into two major part, Firstly,to observe the variance of cough reflex sensitivity of chronic cough patients and the relationship between it and airway inflammation.

1. Recruit chronic cough patients and healthy volunteers as subjects.

2. Help subjects to complete detailed history,physical examination,Hull airway reflux questionnaire,chest x-rays,induced sputum,blood routine test,pulmonary ventilation function test and histamine provocation test before they enter this study.

3. Complete allyl isothiocynate(AITC) cough provocation test the day subjects enter the study,then complete capsaicin(CAP)cough provocation test after 3 days.

4. To detect the substance P(SP),calcitonin gene-related peptide(CGRP),prostaglandin E2(PGE2),et al level in sputum supernatants.

Secondly,to observe the distribution of TRPA1,TRPV1 channels and the relationship between it and cough reflex sensitivity.

1)Recruit chronic cough patients and healthy volunteers and complete related examinations as mentioned before.

2)Collect mucosa specimens from upper trachea via endobronchial biopsy,and airway epithelial cells from 2nd or 3rd order bronchi via brushing.

3)Evaluate the expression level of TRPA1,TRPV1 of mucosa specimens of subjects by immunofluorescent assay and Image analysis software.

4)Cultivate airway epithelial cells from subjects and evaluate the expression of TRPV1,TRPA1 and functional changes of it.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 17 Years to 70 Years
Eligibility Inclusion Criteria:

chronic cough group:

1. cough lasting = 8 weeks,characterized by irritating dry cough.

2. sensitive to fumes,dust,the odorous and cold air.

3. with normal chest x-rays. 4.17-70 years old.

5.without smoking history. healty controls group: 1.17-70 years old. 2.without smoking hitory or stop smoking for more than 2 years. 3.without chronic cough. 4.without chronic respiratory diseases. 5.without chronic heart, liver, kidney,and autoimmune disease. 6.with normal chest x-rays. 7.with normal pulmonary ventilation function,and histamine challenge test showed negative result.

Exclusion Criteria:

chronic cough group and healty controls group:

1. with respiratory tract infection within 8 weeks.

2. with chronic respiratory diseases or severe heart, liver, kidney,and autoimmune disease.

3. using Angiotensin-Converting Enzyme Inhibitors(ACEI),bronchodilators,glucocorticosteroid,antihistaminics within one week.

4. women during pregnancy or lactation.

5. patients with malignant tumours.

Study Design

Observational Model: Case Control


Related Conditions & MeSH terms


Locations

Country Name City State
China Guangzhou Institute of Respiratory Disease Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Kefang Lai

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary TRPA1,TRPV1 channels expression level of chronic cough patients and its relationship with cough reflex sensitivity Complete AITC cough provocation test the day subjects enter the study,then complete CAP cough provocation test after 3 days,record the threshold of cap and aitc concentration(mmol/L) when it cause subjects cough equal to or more than 5 times.Measure the expression level of TRPA1 and TRPV1 of biopsy sample from chronic cough patients and healthy controls by immunofluoresent assay 7 days post bronchoscopy.Analyze the statistic by spss18.0. 7 days post-bronchoscopy No
Secondary The relationship between CAP cough reflex sensitivity test conducted by TRPV1 and AITC cough reflex sensitivity test conducted by TRPA1 Complete AITC cough provocation test the day subjects enter the study,then complete CAP cough provocation test after 3 days,record the threshold of cap and aitc concentration(mmol/L) when it cause subjects cough equal to or more than 5 times.Analyze the statistic by spss18.0. 7 days post-bronchoscopy No
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