Follow-up of Respiratory Sequelae of Hospitalized Patients With COVID-19 : Follow-up of Respiratory Sequelae of Patients Hospitalized With SARS-CoV-2: a Prospective Multicenter Observational Study
Main objective To assess respiratory sequelae after SARS-CoV-2 infection in hospitalized patients with severe pneumonia requiring oxygen supply and followed up for 6 months after hospital discharge (see primary and secondary outcomes).Secondary objectivesTo describe pulmonary sequelae according to :the unit in which the patient was hospitalized,the maximum oxygen flow rate required during hospitalization,McCabe score,age,tobacco consumption,biological data (e.g. blood count, CRP, fibrinogen, LDH, albumin, D-dimer, ferritin),number of days from onset of symptoms to hospitalization,co-morbidities (e.g. diabetes, hypertension, coronary artery disease/heart failure, mild to moderate COPD/respiratory failure, overweight),concomitant treatments (e.g. non-steroidal anti-inflammatory drugs, corticosteroids, immunosuppressants, ACE inhibitors)specific drug treatments administered to treat COVID-19 infection,non-drug treatments (invasive ventilation, non-invasive ventilation, postural treatment) to manage respiratory disorders of COVID-19 infection.To assess the impact of factors of social inequality on the severity of COVID-19 infection.Conduct of research Patients who have been hospitalized for severe pneumonia due to CoV-2 SARS infection will be seen in consultation at approximately 3 and 6 months after hospital discharge, as per standard practice..
Medienart: |
Klinische Studie |
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Erscheinungsjahr: |
2021 |
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Erschienen: |
2021 |
Enthalten in: |
ClinicalTrials.gov - (2021) vom: 16. Dez. Zur Gesamtaufnahme - year:2021 |
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Sprache: |
Englisch |
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Links: |
Volltext [kostenfrei] |
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Themen: |
610 |
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Anmerkungen: |
Source: Link to the current ClinicalTrials.gov record., First posted: August 10, 2020, Last downloaded: ClinicalTrials.gov processed this data on December 27, 2021, Last updated: December 29, 2021 |
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Study ID: |
NCT04505631 |
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Veröffentlichungen zur Studie: |
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fisyears: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
CTG003481891 |
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520 | |a Main objective To assess respiratory sequelae after SARS-CoV-2 infection in hospitalized patients with severe pneumonia requiring oxygen supply and followed up for 6 months after hospital discharge (see primary and secondary outcomes).Secondary objectivesTo describe pulmonary sequelae according to :the unit in which the patient was hospitalized,the maximum oxygen flow rate required during hospitalization,McCabe score,age,tobacco consumption,biological data (e.g. blood count, CRP, fibrinogen, LDH, albumin, D-dimer, ferritin),number of days from onset of symptoms to hospitalization,co-morbidities (e.g. diabetes, hypertension, coronary artery disease/heart failure, mild to moderate COPD/respiratory failure, overweight),concomitant treatments (e.g. non-steroidal anti-inflammatory drugs, corticosteroids, immunosuppressants, ACE inhibitors)specific drug treatments administered to treat COVID-19 infection,non-drug treatments (invasive ventilation, non-invasive ventilation, postural treatment) to manage respiratory disorders of COVID-19 infection.To assess the impact of factors of social inequality on the severity of COVID-19 infection.Conduct of research Patients who have been hospitalized for severe pneumonia due to CoV-2 SARS infection will be seen in consultation at approximately 3 and 6 months after hospital discharge, as per standard practice. | ||
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