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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01801657
Other study ID # 2009CB522109
Secondary ID
Status Recruiting
Phase N/A
First received February 25, 2013
Last updated March 11, 2014
Start date February 2013
Est. completion date April 2014

Study information

Verified date March 2014
Source The First Affiliated Hospital of Guangzhou Medical University
Contact Rongchang Chen, MD
Phone 020-83062718
Email Chenrc@Vip.163.com
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

Bronchiectasis is clinically characterized by irreversible dilation of the bronchi and bronchioles leading to persistent cough, purulent sputum, and airway flow limitation, which may be accompanied by recurrent exacerbations.It has been increasingly recognized that respiratory viruses are mainly responsible for acute exacerbation of chronic pulmonary diseases, i.e. asthma, chronic obstructive pulmonary disease and cystic fibrosis. However,little is known about the roles of viral infection in driving exacerbations of bronchiectasis.This study aims to identify the frequency of common viral infections and determine the roles that viruses play in acute exacerbations of bronchiectasis.


Description:

Bronchiectasis is a chronic airway disease characterised by a vicious cycle of persistent bacterial colonization,inflammation and progressive tissue destruction.Patients with bronchiectasis frequently developed acute exacerbations characterised by acute worsening requiring changes in concomitant use of medication,with attendant adverse effects on their morbidity and health-related quality of life. The detailed pathogenesis of exacerbations of bronchiectasis, however, remains poorly understood.

Recent data suggested that airway infection and inflammation are important drivers of exacerbations,therefore the imbalance between chronic bacterial infection and host immune response may result in bronchiectasis exacerbations. Viral infection may be an important factor that leads to this events.It has been established that respiratory viruses are mainly responsible for the exacerbations of other chronic respiratory diseases, i.e. asthma, COPD and cystic fibosis. However, the data regarding prospective studies that sought to investigate the roles of viruses in acute exacerbation of bronchiectasis are lacking. Furthermore,the associations between viruses and bacteria during exacerbation need to be assessed. This study targets at indentifying the frenquency of common viral infections in adults with non-cystic fibrosis bronchiectasis and may shed light on the effects they have on clinical parameters,i.e. the length of exacerbated symptom to recovery,lung function, pulmonary inflammation, bacterial load and quality of life.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Age = 18 years

- HRCT-diagnosed Bronchiectasis

- Capable of providing written informed consent

Exclusion Criteria:

- Patient judged to have poor compliance

- Cystic fibrosis bronchiectasis

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
The First Affiliated Hospital of Guangzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The prevalence of respiratory virus infection in adults with bronchiectasis during a pulmonary exacerbation and when clinically stable. Respiratory viruses in the nasal swab and sputum will be identified using the polymerase chain reaction(PCR)technique when clinically stable and during exacerbation.The following viruses will be tested for:influenza A,B(including influenza A H1N1),respiratory syncytial virus(RSV),Enterovirus,Parainfluenza 1-4,Rhinovirus,human Coronaviruses(subtypes OC43?229E?HKU1),human metapneumovirus,adenovirus, human bocavirus,chlamydia,mycoplasma. 1 year No
Secondary The effect of respiratory virus infection on systemic and pulmonary inflammatory markers. Systemic and airway inflammatory cytokines including IL-1ß?IL-6?IL-8?TNF-a were measured using a commercial multiplex bead-based assay. 1 year No
Secondary The effect of respiratory virus on lung function Spirometric indices in the present study is referred to as forced expiratory vilume in 1s(FEV1),forced vital capacity(FVC).Spirometry tests are carried out using a spirometer (COSMED, QUARK PFT, Italy). All operation procedures meet the joint recommendation by ATS and ERS. A total of at least 3 (not more than 8) spirometric maneuvers are performed, with the variation between the best two maneuvers of <5% or 200ml in FVC and FEV1. The maximal values of FVC and FEV1 are reported. 1 year No
Secondary The effect of respiratory virus infection on the bacterial load in bronchiectasis. Type of bacterial infection, also referred to as potentially pathogenic organisms, and bacterial load, as expressed in cfu per mililiter 1 year No
Secondary Time to recovery of respective symptom The time from exacerbation onset by which a 3-d moving average was equal to or exceeded the baseline value 1 year No
Secondary The effect of respiratory virus on quality of life in patients with bronchiectasis Quality of life in patients with bronchiectasis were measured by St.George Respiratory Questionnaire?Leicester Cough Questionnaire and COPD assessment test during exacerbations,and then compared between virus-postive and virus-negative patients 1 year No
Secondary To investigate if upper respiratory tract symptoms are associated with viral infections. 1 year No
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