COPDNCT05750810
Exacerbations and Their Outcomes International (EXACOS International)
An observational study of COPD and Exacerbation Copd, run by Joon Young Choi at 1 site in South Korea.
Trial summary
The aim of this study is to quantify the burden of severe AECOPD in South Korea, by investigating the association between frequency of severe AECOPD and clinical and health-care utilization outcomes. Read more about this study
- Who is it for?
- Ages 40 years and older
- Conditions the study is for
- COPD, Exacerbation Copd
- What is being tested?
- Severe exacerbation frequency
- How many people
- 3,477 participants
- Where
- 1 siteSouth Korea
- Study dates
- Apr 2012to Dec 2021
- How long will I take part?
- 10 Years
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: This study was based on the Korea COPD Subgroup Study (KOCOSS) database, constructed from a nationwide prospective cohort study-initiated in April 2012-that involved 54 medical centers in South Korea. It was designed to evaluate characteristics of COPD patients in South Korea.
Who may be able to join
- Over 40 years old South Korean COPD patients(Bronchodilator test results FEV1/FVC <0.7)
- COPD patients who complain of cough, sputum, dyspnea
- Unrelated smoking history
Who cannot join
- other disease like asthma patients which is similar to COPD symptoms.
- patients who is not suitable for pulmonary function test and communication
- myocardial infarction or cerebrovascular event within the previous 3 months
- pregnants
- patients who disagree with registration
- rheumatoid patients
Show all 9Show fewer
- cancer patients(including metastatic cancer, leukemia, lymphoma)
- irritable bowel syndrome
- patients who use systemic steroids over 8 weeks due to other diseases except COPD
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Exacerbations and Their Outcomes International (EXACOS International): Burden of Severe Exacerbations of COPD and the Association Between Frequency of Severe Exacerbations and Clinical and Health-care Utilization Outcomes
The aim of this study is to quantify the burden of severe AECOPD in South Korea, by investigating the association between frequency of severe AECOPD and clinical and health-care utilization outcomes.
Read the detailed description
- BACKGROUND AND RATIONALE Chronic obstructive pulmonary disease (COPD) is a common, progressive disease characterized by airflow obstruction which is not fully reversible. Acute exacerbations of COPD (AECOPD) are worsening of COPD symptoms (breathlessness, cough, and sputum volume and purulence) beyond normal day to day variation. Between 30-50% of patients with COPD experience at least one AECOPD per year [1]. Even a single moderate AECOPD increases risk of future multiple AECOPD events, starting a spiral of excessive disease progression and leading to an increased risk of death [2]. AECOPDs have also been associated with other clinical outcomes such as accelerated lung function decline [3,4]. Studies have shown that AECOPDs are related to future AECOPDs, however, little is known about clinical burden and health care utilization in the COPD population [2, 5]. To date, most of published literature reports a combined category of moderate-severe exacerbations, typically stratifying patients as experiencing frequent (i.e. two or more events per patient-year) vs. infrequent (none or one) exacerbations. The aim of this study is to quantify the burden of severe AECOPD in South Korea, by investigating the association between frequency of severe AECOPD and clinical and health-care utilization outcomes. This study will help to understand the relationship between severe AECOPD and clinical and health care utilization burden in South Korea with no established health care databases.
- OBJECTIVES AND HYPOTHESES The objective is to quantify the burden of severe AECOPD by describing the clinical and health care utilization burden of AECOPD by frequency.
2.1 Primary Objectives
2.1 Primary Objectives \& Hypothesises
- To estimate the frequency of severe AECOPD, in a COPD population
- To describe any time trends in the frequency of severe exacerbations throughout the study period (over a 2-year period)
- To describe lung function decline over time (FEV1)
- To quantify health care resource utilization by number of severe AECOPD over a 2-year period
2.2 Secondary Objective \& Hypothesis
- Modified Medical Research Council (mMRC) dyspnea scale measured at time of the visit
- METHODOLOGY 3.1 Study Design - General Aspects This study was based on the Korea COPD Subgroup Study (KOCOSS) database, constructed from a nationwide prospective cohort study-initiated in April 2012-that involved 54 medical centers in South Korea. During the patient visit, data was captured through the use of Case Report Forms (CRFs) by a doctor or trained nurse. After a baseline evaluation, patients were examined at 1-year follow-up. 3.2 Study Population Inclusion criteria of the KOCOSS database is as follows:
- Age > 40 years; 2) those with post-bronchodilator (FEV1)/forced vital capacity (FVC) ≤ 70% of the normal predicted value. The following subpopulations of interest will be identified:
- Patients with eosinophils ≥100cells/ul
- Patients with a history of a comorbidity of special interest:
- Any history of major cardiovascular comorbidity as recorded in the medical records: AMI, heart failure, stroke (+ MACE)
- Any cardiovascular risk factor as recorded in the medical history: hypertension, diabetes - Any history of other major comorbidity: depression, anxiety, GERD, renal failure, etc. 3.3 Study Period Data of COPD patients from April 2012 to 2021 will be extracted and analyzed
- VARIABLES AND EPIDEMIOLOGICAL MEASUREMENTS 4.1 Exposures The main exposure for this study is severe exacerbation frequency. A severe exacerbation will be primarily defined as a hospitalization (with or without ICU) or an emergency department visit as a result of worsening of COPD symptoms. The number of severe AECOPD was counted at the initial visit in recall of previous 1-year events, and prospectively measured at 1-year follow up visit. The annual severe AECOPD frequency will be estimated in the 2 years (pre- and post- 1-year of initial visit), and divided by 2. This will guide the categorization of the severe AECOPD frequency. We expect the following categories:
- 0 events
- 1 severe event
- 2 severe events
- 3 severe events
- >3 severe events The distribution of exacerbations across the entire 2 year period will also be described. In order to fully describe severe AECOPDs and their impact in disease progression, clinical burden, and healthcare costs the following outcomes will be measured:
- Clinical burden defined as change in lung function (FEV1) over time 2) Co-morbidities 3) Health care utilization burden will be defined accounting for: -number of emergency department visits -number of hospitalizations -number of ICU episodes
- STATISTICAL ANALYSIS PLAN 5.1 Statistical Methods - General Aspects Summary statistics will be provided for the COPD population overall and by sub-populations noted above. Continuous measures will be described using means and standard deviations and categorical measures will be reported using numbers and proportions. Count variables will be expressed as rates per person-year. Groups will be compared using standard univariate statistical methods, including the chi-square test or the Fisher exact test for categorical variables and the analysis of variance test for continuous variables. 5.2 Sample Size and Power Calculations No power calculations were performed as the objectives of this study are mostly descriptive in nature.
- Conditions
- COPD, Exacerbation Copd
- Being tested
- Severe exacerbation frequency
- Medical subject headings
- Pulmonary Disease, Chronic Obstructive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Severe exacerbation frequencyOther
A severe exacerbation will be primarily defined as a hospitalization (with or without ICU) or an emergency department visit as a result of worsening of COPD symptoms.
What is being measured
The primary outcome is the main question the study is designed to answer.
the frequency of severe AECOPD
To estimate the frequency of severe AECOPD, in a COPD population
Measured: 10-year
time trends in the frequency of severe exacerbations
To describe any time trends in the frequency of severe exacerbations throughout the study period (over a 2-year period)
Measured: 2-year
lung function decline over time
To describe lung function decline over time (FEV1)
Measured: 3-year
health care resource utilization
To quantify health care resource utilization by number of severe AECOPD over a 2-year period
Measured: 2-year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Mar 2023
- Study startApr 2012
- Primary completionDec 2021
- Study completionDec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for COPDStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 3,477 participants (actual)
- Target duration
- 10 Years
Sponsor and investigators
- Lead sponsor
- Joon Young Choi
- Sponsor type
- University, hospital or other
- Collaborators
- Seoul St. Mary's Hospital, Hallym University Medical Center, Konkuk University Hospital
- Responsible party
- Sponsor-investigator, Joon Young Choi, Incheon St.Mary's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05750810
- Sponsor's protocol ID
- ESR-21-21659
- Status last verified
- Feb 2023
- First submitted
- 20 Feb 2023
- Last updated
- 2 Mar 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: IPD is not available due to restriction
Publications
Rhee CK, Choi JY, Park YB, Yoo KH. Clinical Characteristics and Frequency of Chronic Obstructive Pulmonary Disease Exacerbations in Korean Patients: Findings From the KOCOSS Cohort 2012-2021. J Korean Med Sci. 2024 May 20;39(19):e164. doi: 10.3346/jkms.2024.39.e164.
PubMed 38769923
Study at a glance
From the registry record, last updated by the sponsor on 2 Mar 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exacerbations and Their Outcomes International (EXACOS International): Burden of Severe Exacerbations of COPD and the Association Between Frequency of Severe Exacerbations and Clinical and Health-care Utilization Outcomes
- ClinicalTrials.gov ID
- NCT05750810
- Acronym / sponsor ID
- ESR-21-21659
- Conditions
- COPD, Exacerbation Copd
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 3,477 participants (actual)
- Lead sponsor
- Joon Young ChoiUniversity, hospital or other
- Collaborators
- Seoul St. Mary's Hospital, Hallym University Medical Center, Konkuk University Hospital
- Study start
- Apr 2012 (actual)
- Primary completion
- Dec 2021 (actual)
- Study completion
- Dec 2021 (actual)
- First posted
- 2 Mar 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to quantify the burden of severe AECOPD in South Korea, by investigating the association between frequency of severe AECOPD and clinical and health-care utilization outcomes.
Detailed description
- BACKGROUND AND RATIONALE Chronic obstructive pulmonary disease (COPD) is a common, progressive disease characterized by airflow obstruction which is not fully reversible. Acute exacerbations of COPD (AECOPD) are worsening of COPD symptoms (breathlessness, cough, and sputum volume and purulence) beyond normal day to day variation. Between 30-50% of patients with COPD experience at least one AECOPD per year [1]. Even a single moderate AECOPD increases risk of future multiple AECOPD events, starting a spiral of excessive disease progression and leading to an increased risk of death [2]. AECOPDs have also been associated with other clinical outcomes such as accelerated lung function decline [3,4]. Studies have shown that AECOPDs are related to future AECOPDs, however, little is known about clinical burden and health care utilization in the COPD population [2, 5]. To date, most of published literature reports a combined category of moderate-severe exacerbations, typically stratifying patients as experiencing frequent (i.e. two or more events per patient-year) vs. infrequent (none or one) exacerbations. The aim of this study is to quantify the burden of severe AECOPD in South Korea, by investigating the association between frequency of severe AECOPD and clinical and health-care utilization outcomes. This study will help to understand the relationship between severe AECOPD and clinical and health care utilization burden in South Korea with no established health care databases.
- OBJECTIVES AND HYPOTHESES The objective is to quantify the burden of severe AECOPD by describing the clinical and health care utilization burden of AECOPD by frequency.
2.1 Primary Objectives
2.1 Primary Objectives \& Hypothesises
- To estimate the frequency of severe AECOPD, in a COPD population
- To describe any time trends in the frequency of severe exacerbations throughout the study period (over a 2-year period)
- To describe lung function decline over time (FEV1)
- To quantify health care resource utilization by number of severe AECOPD over a 2-year period
2.2 Secondary Objective \& Hypothesis
- Modified Medical Research Council (mMRC) dyspnea scale measured at time of the visit
- METHODOLOGY 3.1 Study Design - General Aspects This study was based on the Korea COPD Subgroup Study (KOCOSS) database, constructed from a nationwide prospective cohort study-initiated in April 2012-that involved 54 medical centers in South Korea. During the patient visit, data was captured through the use of Case Report Forms (CRFs) by a doctor or trained nurse. After a baseline evaluation, patients were examined at 1-year follow-up. 3.2 Study Population Inclusion criteria of the KOCOSS database is as follows:
- Age > 40 years; 2) those with post-bronchodilator (FEV1)/forced vital capacity (FVC) ≤ 70% of the normal predicted value. The following subpopulations of interest will be identified:
- Patients with eosinophils ≥100cells/ul
- Patients with a history of a comorbidity of special interest:
- Any history of major cardiovascular comorbidity as recorded in the medical records: AMI, heart failure, stroke (+ MACE)
- Any cardiovascular risk factor as recorded in the medical history: hypertension, diabetes - Any history of other major comorbidity: depression, anxiety, GERD, renal failure, etc. 3.3 Study Period Data of COPD patients from April 2012 to 2021 will be extracted and analyzed
- VARIABLES AND EPIDEMIOLOGICAL MEASUREMENTS 4.1 Exposures The main exposure for this study is severe exacerbation frequency. A severe exacerbation will be primarily defined as a hospitalization (with or without ICU) or an emergency department visit as a result of worsening of COPD symptoms. The number of severe AECOPD was counted at the initial visit in recall of previous 1-year events, and prospectively measured at 1-year follow up visit. The annual severe AECOPD frequency will be estimated in the 2 years (pre- and post- 1-year of initial visit), and divided by 2. This will guide the categorization of the severe AECOPD frequency. We expect the following categories:
- 0 events
- 1 severe event
- 2 severe events
- 3 severe events
- >3 severe events The distribution of exacerbations across the entire 2 year period will also be described. In order to fully describe severe AECOPDs and their impact in disease progression, clinical burden, and healthcare costs the following outcomes will be measured:
- Clinical burden defined as change in lung function (FEV1) over time 2) Co-morbidities 3) Health care utilization burden will be defined accounting for: -number of emergency department visits -number of hospitalizations -number of ICU episodes
- STATISTICAL ANALYSIS PLAN 5.1 Statistical Methods - General Aspects Summary statistics will be provided for the COPD population overall and by sub-populations noted above. Continuous measures will be described using means and standard deviations and categorical measures will be reported using numbers and proportions. Count variables will be expressed as rates per person-year. Groups will be compared using standard univariate statistical methods, including the chi-square test or the Fisher exact test for categorical variables and the analysis of variance test for continuous variables. 5.2 Sample Size and Power Calculations No power calculations were performed as the objectives of this study are mostly descriptive in nature.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 10 Years
Who may qualify
- Ages
- 40 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- This study was based on the Korea COPD Subgroup Study (KOCOSS) database, constructed from a nationwide prospective cohort study-initiated in April 2012-that involved 54 medical centers in South Korea. It was designed to evaluate characteristics of COPD patients in South Korea.
Key inclusion criteria (3 listed)
Key exclusion criteria (9 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Severe exacerbation frequencyA severe exacerbation will be primarily defined as a hospitalization (with or without ICU) or an emergency department visit as a result of worsening of COPD symptoms. | Other | – |
Primary outcome
the frequency of severe AECOPD
Time frame: 10-year
To estimate the frequency of severe AECOPD, in a COPD population
time trends in the frequency of severe exacerbations
Time frame: 2-year
To describe any time trends in the frequency of severe exacerbations throughout the study period (over a 2-year period)
lung function decline over time
Time frame: 3-year
To describe lung function decline over time (FEV1)
health care resource utilization
Time frame: 2-year
To quantify health care resource utilization by number of severe AECOPD over a 2-year period
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Mar 2023.
- Derived from this study: PubMed 38769923Rhee CK, Choi JY, Park YB, Yoo KH. Clinical Characteristics and Frequency of Chronic Obstructive Pulmonary Disease Exacerbations in Korean Patients: Findings From the KOCOSS Cohort 2012-2021. J Korean Med Sci. 2024 May 20;39(19):e164. doi: 10.3346/jkms.2024.39.e164.
- Individual participant dataSharing planned: No. IPD is not available due to restriction
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of COPD and Exacerbation Copd, run by Joon Young Choi at 1 site in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Mar 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
the frequency of severe AECOPD (time frame: 10-year). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05750810, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Mar 2023.