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Argentinian Registry of Patients With Rheumatic Diseases and COVID-19 Infection

Argentinian Registry of Patients With Rheumatic Diseases and COVID-19 Infection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04568421
Acronym
SAR-COVID
Enrollment
2982
Registered
2020-09-29
Start date
2020-08-18
Completion date
2022-12-31
Last updated
2023-02-01

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

Conditions

Rheumatic Diseases

Keywords

COVID-19

Brief summary

SAR-COVID is a national, multicenter, prospective, observational longitudinal registry of consecutive patients with diagnosis of rheumatic diseases treated or not with immunomodulatory and/or immunosuppressive drugs and SARS-CoV-2 infection (asymptomatic or COVID-19). Hypothesis: Patients with rheumatic diseases who are under chronic treatment with immunomodulatory and/or immunosuppressive drugs more frequently have an asymptomatic infection, a milder COVID-19 and lower mortality than patients with rheumatic diseases without immunomodulatory and/or immunosuppressive treatments.

Detailed description

SAR-COVID is a national, multicenter, prospective, observational longitudinal registry of consecutive patients with diagnosis of rheumatic diseases treated or not with immunomodulatory and/or immunosuppressive drugs and SARS-CoV-2 infection (asymptomatic or COVID-19). HYPOTESIS: Patients with rheumatic diseases who are under chronic treatment with immunomodulatory and/or immunosuppressive drugs more frequently have an asymptomatic infection, a milder COVID-19 and lower mortality than patients with rheumatic diseases without immunomodulatory and/or immunosuppressive treatments. TARGET POPULATION: Patients \> 18 years of age with any rheumatic disease. ELIGIBILITY CRITERIA Inclusion Criteria * Age \> 18 years. * Patients with diagnosis of rheumatic diseases (treated or not with immunomodulatory and/or immunosuppressive drugs). * Patients with diagnosis of SARS-CoV-2 infection (past or present) with positive test for the virus SARS-CoV-2 from analysis of nasopharyngeal or oropharyngeal swab specimens (reverse transcriptase-polymerase- chain-reaction assay) or by serology, independently of symptoms. Exclusion Criteria • Patients who do not wish to participate or are unable to give informed consent. RECRUITMENT: All rheumatologists, members of the Argentine Society of Rheumatology will be invited to participate in the registry. It is expected that 3,000 patients with COVID-19 and some rheumatic disease, who are cared for by rheumatologists in any of the 23 provinces of Argentina, will be enrolled in the SAR-COVID registry during the period from July 1 to December 31, 2020. Twelve-month extension of the recruitment period will be applied if the expected number of patients is not achieved by the end of the inclusion date. Two cohorts will be included: the first will enroll 1,500 patients treated with immunomodulatory and/or immunosuppressive drugs, and the second will enroll 1,500 patients without immunomodulatory and/or immunosuppressive drugs. DATA COLLECTION: All variables will be collected by self-report, clinical and laboratory examination and/or medical records review, performed by the rheumatologist during patient hospitalization due to COVID-19, or at the patient control visit performed after SARS-CoV-2 infection. The data will be entered into the ARTHROS eCRF (online application designed ad hoc), which in turn will facilitate generating queries and perform the statistical analysis. PERIODIC REPORTS: Patients will be followed up for 12 months, in order to evaluate their evolution and identify the effect of the SARS-CoV-2 infection on their rheumatological disease. For this reason, in this registry the data will be collected in two phases: * PHASE I: Corresponds to the baseline visit (T0). Sociodemographic data, diagnosis, symptoms, treatment, hospitalization, complications, characteristics of the rheumatic disease and its treatment before and during the infectious process will be recorded. * PHASE II: This second visit (T1) will be carried out 12 months after patients registration. Its objective is to identify long-term complications after SARS-CoV-2 infection and to assess the impact of infection on rheumatic disease.

Interventions

DRUGImmunosuppressive Agents

Immunomodulatory and/or immunosuppressive drugs according to the indication of the treating physician

Sponsors

Sociedad Argentina de Reumatologia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age equal or older than 18 years. * Patients with diagnosis of rheumatic diseases (treated or not with immunomodulatory and/or immunosuppressive drugs). * Patients with diagnosis of SARS-CoV-2 infection (past or present) with positive test for the virus SARS-CoV-2 from analysis of nasopharyngeal or oropharyngeal swab specimens (reverse transcriptase-polymerase- chain-reaction assay) or by serology, independently of symptoms.

Exclusion criteria

* Patients who do not wish to participate or are unable to give informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Mortality2 monthDeath caused by SARS-CoV-2 infection
Hospitalization2 monthHospitalization because of SARS-CoV-2 infection

Secondary

MeasureTime frameDescription
Invasive mechanical ventilation2 monthProportion of patients who required invasive mechanical ventilation
SARS-CoV-2 infection presentation1 monthTo describe clinical presentation of SARS-CoV-2 infection in patients with rheumatic diseases
Recovery rate2 monthProportion of patients fully or partially recovered after COVID-19 infection.
COVID-19 Complications2 monthProportion of patients who had complications associated with COVID-19 infection and describe them
Admission at the intensive care unit2 monthProportion of patients admitted at the intensive care unit

Countries

Argentina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026