Evolution of Coronavirus Disease 2019 (COVID-19) Patients in Extremadura
NCT ID: NCT04724850
Last Updated: 2024-05-08
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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COMPLETED
440 participants
OBSERVATIONAL
2020-07-14
2022-12-30
Brief Summary
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We will carry out a multicenter, observational, descriptive, cross-sectional and longitudinal study of patients diagnosed with SARS-CoV-2 virus infection in the Community of Extremadura to determine the effectiveness of drug treatments and the clinical and evolutionary characteristics of these patients and the different factors that may influence its evolution.
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Detailed Description
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These data will be obtained mainly from the clinical history and collected in the data collection notebooks and electronic base designed for the study for subsequent analysis. The data collection period will be one year, estimating a sample of 5,000 patients.
In addition, patients included in the study prospectively will be asked for consent to collect a blood sample for freezing and storage in the Biobank of Extremadura and subsequent use to determine biomarkers and genetics.
The present study will be carried out in accordance with the observational National Post-Authorization Study (EPA) for medicines for human use proposed by Valdecilla Health Research Institute (IDIVAL), the main objective of which is to determine the effectiveness of the pharmacological treatments currently used in COVID-19.
Conditions
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Study Design
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COHORT
OTHER
Study Groups
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COVID-19 patients
All patients diagnosed with COVID-19 in the community of Extremadura from the beginning of the epidemic to its ending in Spain.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients diagnosed with SARS-Cov2 infection according to the clinical and microbiological criteria established by the Health Authorities and clinical practice (these can be modified based on the Technical document "Clinical management of COVID-19" of the Ministry of Health) who require or not hospitalization and who receive or not specific pharmacologic treatment for the SARS-Cov2 infection.
Exclusion Criteria
ALL
No
Sponsors
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Juan Fernando Masa Jiménez
OTHER
Responsible Party
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Juan Fernando Masa Jiménez
Principal Investigator
Principal Investigators
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Juan F Masa Jiménez, PhD
Role: PRINCIPAL_INVESTIGATOR
Servicio Extremeño de Salud
Locations
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Hospital San Pedro de Alcántara
Cáceres, , Spain
Countries
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Other Identifiers
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1/2020
Identifier Type: -
Identifier Source: org_study_id
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