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Small Airways Evaluation and Treatment

Primary Purpose

Pulmonary Disease,Chronic Obstructive;

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
beclomethasone
formoterol
budesonide
Sponsored by
Zhujiang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease,Chronic Obstructive; focused on measuring Pulmonary disease, chronic obstructive, small airway

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of chronic obstructive pulmonary disease;
  • More than 40 years;

Exclusion Criteria:

  • asthma , or combined with bronchiectasia,pneumonia in the right upper lobe;
  • Malignant tumor in the lung or other parts of the body;
  • Uncontrolled hypertension (systolic blood pressure >200 mmHg, diastolic blood pressure >100 mmHg);
  • Severe cardiac insufficiency, arrhythmia;

Sites / Locations

  • Zhujiang HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

beclomethasone / formoterol

budesonide / formoterol

Arm Description

beclomethasone 100ug and formoterol 6ug , 2 inhalations, twice daily ,for three months

budesonide 160ug and formoterol 4.5ug, 2 inhalations ,twice daily ,for three month

Outcomes

Primary Outcome Measures

R5-R20 measured by IOS
Change of small airway resistance (R5-R20)measured by IOS at three months

Secondary Outcome Measures

forced expiratory volume at one second(FEV1)
change of forced expiratory volume at one second(FEV1) measured by pulmonary function test(PFT)at three months
Score of symptoms using the St. George respiratory questionnaire
The St. George respiratory questionnaire
Score of symptoms using modified Medical Research Council Dyspnoea Scale(mMRC)
modified Medical Research Council Dyspnoea Scale(mMRC)
Score of symptoms
CAT
Change of wall thickness(WT)
change of thickness of the third stage branches of apical segmental bronchus in the right upper lobe (WT) in three months

Full Information

First Posted
August 10, 2015
Last Updated
August 17, 2015
Sponsor
Zhujiang Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02526758
Brief Title
Small Airways Evaluation and Treatment
Official Title
Evaluation and Treatment of Small Airways in COPD
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Unknown status
Study Start Date
April 2015 (undefined)
Primary Completion Date
May 2016 (Anticipated)
Study Completion Date
May 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhujiang Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is a common disease , and characterized by progressive development of airflow limitation. Small airway disease (obstructive bronchitis) and lung parenchyma damage (emphysema) are the main mechanisms of chronic airflow limitation. Research shows that small airway resistance increased by 4-40 times in COPD patients, and become the main part of the airflow obstruction. Impulse oscillation system (IOS) is able to measure the total airway resistance, the central airway resistance and the peripheral airway resistance, which is now widely used to assess small airway function in COPD patients. While High resolution CT (HRCT) is easy to operate and its images are intuitive. Meanwhile it can measure the proportion of emphysema, the airway diameter and the thickness of airway wall. Both of these two tests have great significance in small airway evaluation. Chronic obstructive pulmonary disease with acute exacerbation (AECOPD) is an acute onset process, which is characterized by the aggravation of respiratory symptoms and deterioration of pulmonary function. However, the structural and functional changes of small airway in AECOPD are not clear. Inhalation drugs are the main treatment for stable COPD , and inhaled corticosteroid(ICS)+long-acting beta2-agonist(LABA) are used to treat patients with severe and severe airflow limitation. The particles in traditional inhalation drugs are larger and mainly deposited in large airways, and their effects on small airway function are relatively small. The objectives of the investigators study are COPD patients. The study is divided into two parts, that is the part of AECOPD patients and the part of stable patients . Patients with AECOPD are arranged to take HRCT and IOS test to assess the small airway changes.Patients with stable COPD are randomized to take either beclomethasone / formoterol (particle diameter for 1.4-1.5um) or budesonide / formoterol (3.2um) for three months. The structure and function changes of small airway in different stage will be evaluated and the efficacy of these two drugs is to be compared. This study is expected to highlight the investigators understanding on the role of small airways in COPD, and provide a guideline to clinical standardized treatment as well as evaluation of patients' conditions.
Detailed Description
The COPD patients in the investigators hospital are selected to participate in the investigators study, and strict inclusion and exclusion criteria are to be complied with. All the subjects will be told the details of the study and sign the informed consent before inclusion.HRCT will be used to evaluate the structure of small airway by measuring the thickness of the third stage branches of apical segmental bronchus in the right upper lobe (WT). R5-R20 measured by IOS will be used to assess small airway resistance. The study is divided into two parts, that is the part of AECOPD patients and the part of stable patients . Both of them have three steps . Part 1. AECOPD patients: Subjects screening : To inquire the history of the disease and to take the IOS and Bronchial dilation test. Baseline data collection:patients will be arranged to complete a series of questionnaires, as well as HRCT, IOS, pulmonary function test and 6 minute walk test. Test stage:During their hospital stay, the patients are to be treated with oxygen inhalation and different kinds of drugs, and the patients will followed up for three weeks after discharge. Completing the examinations and questionnaires at each time visit ,and another CT scan at the last visit. Part 2. Stable COPD patients: Subjects screening : To inquire the history of the disease and to take the IOS and Bronchial dilation test. Baseline data collection:In the two-week washout period,patients are only allowed take salmeterol/fluticasone 50:250ug 2 times daily, and stop the use of other inhalation drugs and oral glucocorticoid. At the end of this period, complete a series of questionnaires, as well as HRCT, IOS, pulmonary function test and 6 minute walk test. Test stage: patients are randomized to take either beclomethasone / formoterol (100:6ug 2inhalations twice daily ) or budesonide / formoterol (160:4.5ug 2inhalations twice daily) for three months.Completing the examinations and questionnaires at the end of each month, another CT scan at the last visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease,Chronic Obstructive;
Keywords
Pulmonary disease, chronic obstructive, small airway

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
beclomethasone / formoterol
Arm Type
Experimental
Arm Description
beclomethasone 100ug and formoterol 6ug , 2 inhalations, twice daily ,for three months
Arm Title
budesonide / formoterol
Arm Type
Active Comparator
Arm Description
budesonide 160ug and formoterol 4.5ug, 2 inhalations ,twice daily ,for three month
Intervention Type
Drug
Intervention Name(s)
beclomethasone
Other Intervention Name(s)
Beclomethasone Dipropionate,BDP
Intervention Type
Drug
Intervention Name(s)
formoterol
Intervention Type
Drug
Intervention Name(s)
budesonide
Primary Outcome Measure Information:
Title
R5-R20 measured by IOS
Description
Change of small airway resistance (R5-R20)measured by IOS at three months
Time Frame
three month
Secondary Outcome Measure Information:
Title
forced expiratory volume at one second(FEV1)
Description
change of forced expiratory volume at one second(FEV1) measured by pulmonary function test(PFT)at three months
Time Frame
three month
Title
Score of symptoms using the St. George respiratory questionnaire
Description
The St. George respiratory questionnaire
Time Frame
three month
Title
Score of symptoms using modified Medical Research Council Dyspnoea Scale(mMRC)
Description
modified Medical Research Council Dyspnoea Scale(mMRC)
Time Frame
three month
Title
Score of symptoms
Description
CAT
Time Frame
three month
Title
Change of wall thickness(WT)
Description
change of thickness of the third stage branches of apical segmental bronchus in the right upper lobe (WT) in three months
Time Frame
three month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of chronic obstructive pulmonary disease; More than 40 years; Exclusion Criteria: asthma , or combined with bronchiectasia,pneumonia in the right upper lobe; Malignant tumor in the lung or other parts of the body; Uncontrolled hypertension (systolic blood pressure >200 mmHg, diastolic blood pressure >100 mmHg); Severe cardiac insufficiency, arrhythmia;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shuhan Wu, Master
Phone
13268268627
Email
664397041@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huizhen Fan, Doctor
Organizational Affiliation
Zhujiang Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Zhujiang Hospital
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510280
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shuhan Wu, Master
Phone
13268268627
Email
664397041@qq.com

12. IPD Sharing Statement

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Small Airways Evaluation and Treatment

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