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NCT05770440: EspirCOVID

Impact of COVID-19 on Lung Function in COPD Patients.

Status unknown Last updated 21 March 2023
What this trial tests

trial in COPD in 250 participants. Status unknown.

Timeline
1 March 2023
Primary endpoint
30 June 2023
31 December 2025

Quick facts

Lead sponsorFundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment250
Start date1 March 2023
Primary completion30 June 2023
Estimated completion31 December 2025
Sites1 location across Spain

Conditions studied

Sponsor

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina — full company profile →

Who can join

18 and older, any sex, with COPD or COVID-19. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Background: In 2019, a novel coronavirus (SARS-COV2) was detected in Wuhan, China as a cause of acute respiratory distress syndrome (COVID-19). Other previous coronaviruses (SARS and MERS) have caused respiratory sequelae (pulmonary fibrosis) demonstrable by tomography and lung function tests. These alterations have begun to be detected in patients who have survived COVID-19. Hypotheses: SARS-COV2 infection accelerates the deterioration of lung function in patients with Chronic Obstructive Pulmonary Disease (COPD). Objectives: To analyze the evolution of lung function in COPD patients diagnosed with COVID-19, while comparing it with COPD patients without COVID-19 disease. Methodology: Cohort study. The COPD-COVID-19 cohort will consist of the COPD population with and without COVID-19. Previous pulmonary function data will be collected and 2 prospective visits (baseline and follow-up) with clinical assessments and functional tests will be performed. In the event that the participant suffers from COVID-19 during the follow-up, an additional visit will be performed 3 months after the diagnosis, and the final visit will take place 12 months after this additional visit. Determinations: Study factor: diagnosis of COVID-19. Response variable: change in the forced expiratory volume in the first second (FEV1) measured at the start of the study and after 1 year of this first assessment, considering also the basal FEV1 (before March 2020). Other variables: socio-demographic, clinical, functional and treatment. Expected results: Greater decrease in FEV1 in COPD patients with COVID-19, Applicability and Relevance: The proactive detection of functional sequelae will allow early treatment, including pulmonary rehabilitation, with the aim of improving the quality of life of these patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

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