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A 1-year Multi-center, Prospective, Cohort Study in Patients With Chronic Obstructive Pulmonary Disease Treated With Long-acting Bronchodilator

Primary Purpose

COPD

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
LABA based treatment: indacaterol
LAMA based treatment: tiotropium
LABA/ICS based treatment: salmeterol/fluticasone
LABA/ICS based treatment: budesonide/formoterol
theophylline based treatment
Other treatment
Sponsored by
Novartis Pharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COPD focused on measuring COPD, Chronic obstructive pulmonary disease (COPD),, Chronic obstructive lung disease (COLD),, Chronic obstructive airway disease (COAD),, Cronchitis,, Emphysema

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Willing and able to provide informed consent
  • Physician-diagnosis of COPD
  • COPD patients requiring long-acting bronchodilator treatment
  • Patients with spirometry available at baseline

Exclusion Criteria:

  • Patients who have a diagnosis of asthma.
  • Patients who had been hospitalized for a COPD exacerbation in the 4 weeks prior to Visit 1.
  • Current clinical diagnosis of other chronic respiratory illnesses
  • Concurrent participation in a clinical trial or use of an investigational drug.
  • Active malignancy or history of malignancy of any organ system
  • Pregnant or nursing (lactating) women
  • Women of child-bearing potential with no contraception Other protocol-defined inclusion/exclusion criteria may apply.

Sites / Locations

  • Novartis Investigative Site
  • Novartis Investigative Site

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Indacaterol

Tiotropium Bromide

Salmeterol/Fluticasone

Budesonide/ formoterol

Indacaterol +Tiotropium

LABA/ICS (Or budesonide/ formoterol)+ Tiotropium

Oral theophylline

Other treatment

Arm Description

LABA: Indacaterol, once a day, 150μg each time

LAMA: Tiotropium Bromide, once a day, 18 μg

LABA/ICS: Salmeterol/Fluticasone, twice a day, 50/250 μg, 50/500 μg

Budesonide/formoterol, twice daily, two suction each time, 160/4.5 μg

Indacaterol, once a day, 150μg each time +Tiotropium Bromide, once a day, 18 μg

Salmeterol / fluticasone Or budesonide / formoterol

non-long-acting bronchodilators for COPD treatment, such treatments were classified as "other treatments"

Outcomes

Primary Outcome Measures

Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. A positive change from baseline in FEV1 indicates improvement in lung function. Pulmonary function tests were performed at study visits including FEV1, and Force Vital Capacity (FVC). These were performed 30 minutes before treatment and not more than 2 hours in advance after stopping the Long-acting bronchodilators eight hours before visits. In order to reduce the variation between each test, the same instrument was used in the whole research process if condition allowed.

Secondary Outcome Measures

Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. A positive change from baseline in FEV1 indicates improvement in lung function. Pulmonary function tests were performed at study visits including FEV1, and Force Vital Capacity (FVC). These were performed 30 minutes before treatment and not more than 2 hours in advance after stopping the long-acting bronchodilators eight hours before visits. In order to reduce the variation between each test, the same instrument was used in the whole research process if condition allowed.
COPD Exacerbation
Number of COPD exacerbations evaluated over 12 months. COPD exacerbation is defined as a new onset or worsening of at least 1 respiratory major symptoms (e.g. dyspnea, cough, sputum volume or sputum purulence) for at least 3 consecutive days, which results in recorded treatment change (antibiotics/steroids/oxygen therapy) OR recorded COPD related hospitalization/Emergency visit. COPD exacerbation is not considered as adverse event, and should only be recorded in COPD e-CRF.
Change in Health Status Questionnaire MMRC
The mMRC scale is scored from 0 (less severe) to 4 (severe). 0 Not troubled with breathlessness except with strenuous exercise; 1 Troubled by shortness of breath when hurrying on the level or walking up a slight hill; 2 Walks slower than people of the same age on the level because of breathlessness or has to stop for breath when walking at own pace on the level; 3 Stops for breath after walking about 100 yards or after a few minutes on the level; 4 Too breathless to leave the house or breathless when dressing or undressing. The modified Medical Research Council (mMRC) Dyspnea Scale , is a five-item instrument (part of the Borg scale) to assess a patient's degree of breathlessness in relation to physical activity. Participants will be required to read a brief description of an activity and then select a statement that best describes their experience with dyspnea at Visit 101. The mMRC was assessed by the investigators at the scheduled visits.
Change From Baseline in Questionnaire COPD Assessment Test (CAT) Score
The COPD assessment test (CAT) is a short instrument scale used to quantify the symptom burden of COPD and will be used to assess the health status of patients in this study. It consists of eight items, each presented as a semantic 6-point differential scale, providing a total score out of 40. A higher score indicates a worse health status. Scores of 0 - 10, 11 - 20, 21 - 30 and 31 - 40 represent a mild, moderate, severe or very severe clinical impact of COPD upon the patient.
Change From Baseline Questionnaire Transition Dyspnea Index (TDI) Score
Transition Dyspnea Index (TDI) captures changes from baseline. The TDI score is based on three domains with each domain scored from -3 (major deterioration) to +3 (major improvement), to give an overall score of -9 to +9, a negative score indicating a deterioration from baseline. A TDI focal score of 1 is considered to be a clinically significant improvement from baseline. BDI/TDI was used to assess dyspnea from several aspects, caused by daily activities. These were evaluated by the investigators in the study at the scheduled study visits. The indices were to be evaluated by the same investigator.as far as possible.

Full Information

First Posted
February 15, 2013
Last Updated
August 27, 2019
Sponsor
Novartis Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT01794780
Brief Title
A 1-year Multi-center, Prospective, Cohort Study in Patients With Chronic Obstructive Pulmonary Disease Treated With Long-acting Bronchodilator
Official Title
A 1-year Multi-center, Prospective, Cohort Study in Patients With Chronic Obstructive Pulmonary Disease Treated With Long-acting Bronchodilator
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
February 5, 2013 (Actual)
Primary Completion Date
May 25, 2015 (Actual)
Study Completion Date
May 25, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Novartis Pharmaceuticals

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This multi-center study is designed to describe natural history of disease, treatment and health care products in physician-diagnosed COPD patients who require adding daily maintenance therapy in real world. The study planned to enroll 550 patients in Indacaterol group and 9450 patients in non- Indacaterol group, a total of 10,000 patients. Enrollment was stopped at 2253 patients due to low recruitment in indacaterol group. Finally a total of 2229 patients were analyzed in full analysis set. A total of 2253 patients entered into the database, of which 24 patients were exclude during the data review meetings, because they did not met the inclusion/exclusion criteria. Hence a total of 2229 patients enrolled successfully.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
COPD, Chronic obstructive pulmonary disease (COPD),, Chronic obstructive lung disease (COLD),, Chronic obstructive airway disease (COAD),, Cronchitis,, Emphysema

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
2229 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Indacaterol
Arm Type
Experimental
Arm Description
LABA: Indacaterol, once a day, 150μg each time
Arm Title
Tiotropium Bromide
Arm Type
Experimental
Arm Description
LAMA: Tiotropium Bromide, once a day, 18 μg
Arm Title
Salmeterol/Fluticasone
Arm Type
Experimental
Arm Description
LABA/ICS: Salmeterol/Fluticasone, twice a day, 50/250 μg, 50/500 μg
Arm Title
Budesonide/ formoterol
Arm Type
Experimental
Arm Description
Budesonide/formoterol, twice daily, two suction each time, 160/4.5 μg
Arm Title
Indacaterol +Tiotropium
Arm Type
Experimental
Arm Description
Indacaterol, once a day, 150μg each time +Tiotropium Bromide, once a day, 18 μg
Arm Title
LABA/ICS (Or budesonide/ formoterol)+ Tiotropium
Arm Type
Experimental
Arm Description
Salmeterol / fluticasone Or budesonide / formoterol
Arm Title
Oral theophylline
Arm Type
Experimental
Arm Title
Other treatment
Arm Type
Experimental
Arm Description
non-long-acting bronchodilators for COPD treatment, such treatments were classified as "other treatments"
Intervention Type
Drug
Intervention Name(s)
LABA based treatment: indacaterol
Intervention Description
LABA based treatment: indacaterol
Intervention Type
Drug
Intervention Name(s)
LAMA based treatment: tiotropium
Intervention Description
LAMA based treatment: tiotropium
Intervention Type
Drug
Intervention Name(s)
LABA/ICS based treatment: salmeterol/fluticasone
Intervention Description
LABA/ICS based treatment: salmeterol/fluticasone
Intervention Type
Drug
Intervention Name(s)
LABA/ICS based treatment: budesonide/formoterol
Intervention Description
LABA/ICS based treatment: budesonide/formoterol
Intervention Type
Drug
Intervention Name(s)
theophylline based treatment
Intervention Description
theophylline based treatment
Intervention Type
Drug
Intervention Name(s)
Other treatment
Intervention Description
non-long-acting bronchodilators for COPD treatment, such treatments were classified as "other treatments"
Primary Outcome Measure Information:
Title
Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
Description
Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. A positive change from baseline in FEV1 indicates improvement in lung function. Pulmonary function tests were performed at study visits including FEV1, and Force Vital Capacity (FVC). These were performed 30 minutes before treatment and not more than 2 hours in advance after stopping the Long-acting bronchodilators eight hours before visits. In order to reduce the variation between each test, the same instrument was used in the whole research process if condition allowed.
Time Frame
Baseline,3 months
Secondary Outcome Measure Information:
Title
Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
Description
Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. A positive change from baseline in FEV1 indicates improvement in lung function. Pulmonary function tests were performed at study visits including FEV1, and Force Vital Capacity (FVC). These were performed 30 minutes before treatment and not more than 2 hours in advance after stopping the long-acting bronchodilators eight hours before visits. In order to reduce the variation between each test, the same instrument was used in the whole research process if condition allowed.
Time Frame
Baseline,12 months
Title
COPD Exacerbation
Description
Number of COPD exacerbations evaluated over 12 months. COPD exacerbation is defined as a new onset or worsening of at least 1 respiratory major symptoms (e.g. dyspnea, cough, sputum volume or sputum purulence) for at least 3 consecutive days, which results in recorded treatment change (antibiotics/steroids/oxygen therapy) OR recorded COPD related hospitalization/Emergency visit. COPD exacerbation is not considered as adverse event, and should only be recorded in COPD e-CRF.
Time Frame
Baseline,12 months
Title
Change in Health Status Questionnaire MMRC
Description
The mMRC scale is scored from 0 (less severe) to 4 (severe). 0 Not troubled with breathlessness except with strenuous exercise; 1 Troubled by shortness of breath when hurrying on the level or walking up a slight hill; 2 Walks slower than people of the same age on the level because of breathlessness or has to stop for breath when walking at own pace on the level; 3 Stops for breath after walking about 100 yards or after a few minutes on the level; 4 Too breathless to leave the house or breathless when dressing or undressing. The modified Medical Research Council (mMRC) Dyspnea Scale , is a five-item instrument (part of the Borg scale) to assess a patient's degree of breathlessness in relation to physical activity. Participants will be required to read a brief description of an activity and then select a statement that best describes their experience with dyspnea at Visit 101. The mMRC was assessed by the investigators at the scheduled visits.
Time Frame
Baseline,3,6,9,12 months
Title
Change From Baseline in Questionnaire COPD Assessment Test (CAT) Score
Description
The COPD assessment test (CAT) is a short instrument scale used to quantify the symptom burden of COPD and will be used to assess the health status of patients in this study. It consists of eight items, each presented as a semantic 6-point differential scale, providing a total score out of 40. A higher score indicates a worse health status. Scores of 0 - 10, 11 - 20, 21 - 30 and 31 - 40 represent a mild, moderate, severe or very severe clinical impact of COPD upon the patient.
Time Frame
Baseline,3,6,9,12 months
Title
Change From Baseline Questionnaire Transition Dyspnea Index (TDI) Score
Description
Transition Dyspnea Index (TDI) captures changes from baseline. The TDI score is based on three domains with each domain scored from -3 (major deterioration) to +3 (major improvement), to give an overall score of -9 to +9, a negative score indicating a deterioration from baseline. A TDI focal score of 1 is considered to be a clinically significant improvement from baseline. BDI/TDI was used to assess dyspnea from several aspects, caused by daily activities. These were evaluated by the investigators in the study at the scheduled study visits. The indices were to be evaluated by the same investigator.as far as possible.
Time Frame
Baseline,3,6,9,12 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Willing and able to provide informed consent Physician-diagnosis of COPD COPD patients requiring long-acting bronchodilator treatment Patients with spirometry available at baseline Exclusion Criteria: Patients who have a diagnosis of asthma. Patients who had been hospitalized for a COPD exacerbation in the 4 weeks prior to Visit 1. Current clinical diagnosis of other chronic respiratory illnesses Concurrent participation in a clinical trial or use of an investigational drug. Active malignancy or history of malignancy of any organ system Pregnant or nursing (lactating) women Women of child-bearing potential with no contraception Other protocol-defined inclusion/exclusion criteria may apply.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Novartis Pharmaceuticals
Organizational Affiliation
Novartis Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Novartis Investigative Site
City
Beijing
ZIP/Postal Code
100730
Country
China
Facility Name
Novartis Investigative Site
City
Zhengzhou
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
25474373
Citation
Han J, Dai L, Zhong N, Young D. Breathlessness or health status in chronic obstructive pulmonary disease: the impact of different definitions. COPD. 2015 Apr;12(2):115-25. doi: 10.3109/15412555.2014.974741. Epub 2014 Dec 4.
Results Reference
derived

Learn more about this trial

A 1-year Multi-center, Prospective, Cohort Study in Patients With Chronic Obstructive Pulmonary Disease Treated With Long-acting Bronchodilator

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