Prospective and Multicentric Cohort Study of Severe and Very Severe Chronic Obstructive Pulmonary Disease (COPD) in Brazil (SCOPe).
NCT ID: NCT06724315
Last Updated: 2025-06-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
693 participants
OBSERVATIONAL
2025-01-31
2026-12-15
Brief Summary
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The disease also has a high morbidity leading to impairment in daily activity and quality of life.
Patients with severe and very severe disease are at a higher risk for negative outcomes, including exacerbation (up to 2-3 per patient per year). This in turn increases the risk of future exacerbations and mortality, with heightened risk lasting up to two years after each event. It is impertive to evaluate which sub-groups are at an even higher risk and could be potential targets for intervention.
"The PLATINO study" was conducted on 2004 and evaluated the prevalence of COPD in 5 cities, only one in Brazil - Sao Paulo. As the data is 20 years old it might not reflect the current epidemiological status and might not be representative of Brazil as a whole.
Understanding this population, their clinical and laboratorial characteristics can help identify sub-groups with higher risk and potential for intervention. The current prevalence, causing agent and characteristics are not known in Brazil as well as detailed outcome data.
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Detailed Description
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The patients will be enrolled in non-random consecutive method and will be followed up for 12 months. There will be on-site visits at inclusion (V0), 6 and 12 months. There will tele-consults at 3 and 9 months to gather relevant clinical data, with special interest at exacerbation.
There will be 8 participating centres in Brazil, representing all 5 regions (North, Northeast, Midwest, Southeast and South). They will be Teaching Hospitals, Regional Reference Hospitals, Tertiary Hospitals or High Complexity Hospitals. The data will be collected on each site and will be adjudicated by the ARO Team.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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GOLD B; OR GOLD E
Criteria: CAT ≥10 or MMRC ≥ 2 ; OR 2 exacerbations/year or 1 exacerbation leading to hospitalization
No interventions assigned to this group
GOLD 3 OR 4
Criteria: FVE1 \< 50%
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* GOLD B (mMRC\>=2, CAT\>=10), OR
* GOLD E (\>=2 moderate exacerbations or 1 severe), OR
* GOLD 3 and 4 (FEV1 \<50%).
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Hospital Israelita Albert Einstein
OTHER
Responsible Party
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Principal Investigators
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Henrique AR Fonseca, ScD
Role: STUDY_CHAIR
Hospital Albert Einstein
Locations
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Hospital Israelita Albert Einstein (HIAE)
São Paulo, São Paulo, Brazil
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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SCOPe
Identifier Type: -
Identifier Source: org_study_id
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