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Hospitalary Chronic Obstructive Pulmonary Disease Registry

Hospitalary Chronic Obstructive Pulmonary Disease Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02659189
Enrollment
300
Registered
2016-01-20
Start date
2016-07-31
Completion date
2020-01-31
Last updated
2019-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD Exacerbations, Death

Brief summary

The purpose of this study is to create an institutional registry of Chronic Obstructive Pulmonary disease through a prospective survey based on epidemiological data, risk factors, diagnosis, prognosis, treatment, monitoring and survival.

Detailed description

The main goal is to describe the characteristics of chronic obstructive pulmonary disease patients, including their clinical, spirometric, exacerbation and mortality characteristics within the population of the Hospital Italiano de Buenos Aires.

Interventions

None listed

Sponsors

Hospital Italiano de Buenos Aires
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients older than 40 years with a chronic obstructive pulmonary disease diagnosis according to global obstructive lung Global initiative for chronic Obstructive Lung Disease criteria. * Follow up at the Hospital Italiano de Buenos Aires.

Exclusion criteria

* Refusal to participate or to agree to the informed consent. * Known non chronic obstructive pulmonary disease respiratory disease (ej: Lung Cancer, Tuberculosis, Pulmonary Fibrosis, Neumoconiosis, Cystic Fibrosis, Sarcoidosis, etc) * Severe alpha-1 antitripsin deficit (typr SZ or ZZ) * Previously thoracic surgery (ej: lung volume reduction, lung transplantation).

Design outcomes

Primary

MeasureTime frameDescription
DeathAt 6 months after enrollmentAll cause of death

Secondary

MeasureTime frameDescription
MorbidityAt 6 months after enrollmentSaint George respiratory questionnaire
Functional decline (Forced expired volume at one second)At 12 months after enrollmentForced expired volume at one second
Exacerbations (defined as an increase in symptoms that requires treatment)At 12 months after enrollmentNumber of exacerbations in the timeframe (defined as an increase in symptoms that requires treatment)

Countries

Argentina

Contacts

Primary ContactDiego H Giunta, MD
diego.giunta@hospitalitaliano.org.ar541149590200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026