Name (Synonyms) | Correlation | |
---|---|---|
drug157 | COVID-19 infection Wiki | 0.71 |
drug146 | CHLORPROMAZINE (CPZ) Wiki | 0.71 |
drug669 | Questionnaire by phone call Wiki | 0.71 |
drug148 | COVID 19 diagnostic test by PCR Wiki | 0.71 |
drug773 | Standard of Care (SOC) Wiki | 0.71 |
Name (Synonyms) | Correlation | |
---|---|---|
D001168 | Arthritis NIH | 0.82 |
D008180 | Lupus Erythematosus, Systemic NIH | 0.82 |
D001167 | Arteritis NIH | 0.71 |
D025241 | Spondylarthritis NIH | 0.71 |
D011111 | Polymyalgia Rheumatica NIH | 0.71 |
D013700 | Giant Cell Arteritis NIH | 0.71 |
D012859 | Sjogren's Syndrome NIH | 0.71 |
D003095 | Collagen Diseases NIH | 0.50 |
D001327 | Autoimmune Diseases NIH | 0.50 |
D012216 | Rheumatic Diseases NIH | 0.50 |
Name (Synonyms) | Correlation |
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There are 2 clinical trials
The trial is a prospective, observational study aiming to identify risk factors for serious COVID-19 infection by evaluating clinical measures and biomarkers of inflammation in patients with inflammatory rheumatic disease hospitalized with COVID-19 compared with control groups.
Description: The objective is to examine whether increased disease activity leads to increased risk of hospitalization due to COVID-19 in patients with inflammatory rheumatic disease
Measure: Disease activity Time: Last registration of disease activity in the medical journal before admission/inclusionDescription: Examine whether immune modulating treatments protect or leads to increased risk of hospitalization due to COVID-19 in patients with inflammatory rheumatic disease.
Measure: Immune modulating treatments Time: Current immune modulating treatments at admission/inclusionDescription: Identify prognostic biomarkers by comparing serology of patients with inflammatory rheumatic disease hospitalized with COVID-19 and comparing them with the two control groups
Measure: Biomarkers Time: Blood sample 1 is taken 0-3 days after inclusion and blood sample 2 is taken 2-6 weeks after blood sample 1This epidemiological, transversal, cohort study aims to determine the potential influence of an active long-term hydroxychloroquine intake over the prevalence of a history of symptoms evocative of a COVID-19 infection in patients with a history of systemic lupus erythematosus, rheumatoid arthritis, Sjogren's syndrome or psoriatic arthritis, during the epidemic period in France. The information is gathered using a standardized questionnaire, by phone call.
Description: Adjusted Odds Ratio measuring the association between an exposure to long-term hydroxychloroquine intake and a history of symptoms compatible with a COVID-19 infection.
Measure: Adjusted Odds Ratio Time: 4 months after inclusion