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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04953611
Other study ID # 2013116
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2013
Est. completion date November 30, 2014

Study information

Verified date June 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To explore the HRCT phenotype of the combined COPD assessment staging system


Description:

HRCT can be rapidly and safely deployed has enabled COPD research to move beyond FEV1 by facilitating and amplifying clinical phenotyping measurements, providing quantitative information, and detecting significant responses to therapy even in the absence of significant FEV1 improvements. We explore the HRCT phenotype of the combined COPD assessment staging system,and found that: 1. Airway remodeling occurs in COPD patients. CT shows varying degrees of bronchial wall thickness, area increasing and emphysema as the new GOLD classification Group A-D arising. 2. The GOLD Combined assessment staging system helps doctors choose an individualized treatment for the COPD patients


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date November 30, 2014
Est. primary completion date November 30, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: 1. Age between 40 and 80 (including 40 and 80) 2. It meets the diagnostic criteria for COPD 3. No language communication barriers, or the family members who know the condition can complete the questionnaire on behalf of the patient, and the data are reliable; 4. Voluntarily agree to participate in this study Exclusion Criteria: 1. Older than 80 or younger than 40 2. Pregnant women 3. Complicating with other lung diseases, such as asthma, pneumonia, bronchiectasis, lung abscess, interstitial lung disease, confirmed and suspected lung cancer of lung shadow, active pulmonary tuberculosis, etc 4. Previous lung surgery 5. Cognitive dysfunction 6. Unable to cooperate with lung function test.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Peking University Third Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The severity of emphysema % low attenuation area <950 HU (LAA %) Within an average of 3 days after diagnosis of COPD
Primary Indicator A of the severity of airway stenosis The inner diameter of bronchial (LD) in centimeter Within an average of 3 days after diagnosis of COPD
Primary Indicator B of the severity of airway stenosis The bronchial wall thickness in centimeter Within an average of 3 days after diagnosis of COPD
Primary Indicator C of the severity of airway stenosis Ratio of thickness and outer diameter (TDR) Within an average of 3 days after diagnosis of COPD
Primary Indicator D of the severity of airway stenosis % wall area for bronchial external diameter (WA%) Within an average of 3 days after diagnosis of COPD
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