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| Name | Class |
|---|---|
| Fundación Pública Andaluza para la gestión de la Investigación en Sevilla | OTHER |
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SAM-COVID is a retrospective cohort study that aims to determine the impact of immunosuppressive drugs and immunoglubulins in the outcome of patients with COVID-19.
SAM-COVID is a retrospective cohort study of patients admitted to 66 Spanish hospitals with laboratory-confirmed COVID-19 infection by real-time polymerase chain reaction (RT-PCR) assay for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) presenting during admission with clinical and laboratory data suggestive of macrophage activation syndrome with the objective to investigate whether the use of immunosuppressive drugs (including high-dose steroids, tocilizumab, sarilumab, anakimra) or immunoglobulins in avoiding the need for invasive mechanical ventilation or in-hospital death.
The Ethics Committee for Research of Virgen Macarena and Virgen del Rocío University Hospitals approved the study and waived the need to obtain informed consent.
The data source was the electronic medical records. All data were entered directly by personnel at each institution using an online case report form (CRF), that satisfied local requirements of data confidentiality.
The variables registered included administrative data, epidemiological information, type of clinical specimen in which the diagnosis was confirmed, demographics, comorbidities and current medications, signs and symptoms at admission, baseline laboratory tests results and at day 0, chest X-ray findings at baseline and during follow-up, medications with potential activity against COVID-19, supportive treatments including oxygen therapy, use of immunosuppressant medications or immunoglobulins, and outcome.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| COVID-19 infection | Consecutive patients admitted to Spanish hospitals with laboratory-confirmed COVID-19 infection by real-time polymerase chain reaction (RT-PCR) assay for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) who showed clinical and analytical data suggestive of macrophage activation syndrome during admission until March 30, 2020 . |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NO-Immunosuppressive | Drug | Patients not receiving immunosuppressive drugs |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Invasive ventilation or death | Days until invasive mechanical ventilation or death, whatever happened first. | Up to 21 days |
| Measure | Description | Time Frame |
|---|---|---|
| Ventilation | Days until mechanical ventilation | Up to 21 days |
| Death | Days until death | Up to 21 days |
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Inclusion Criteria:
Clinical criteria:
Laboratory criteria:
Exclusion Criteria:
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Consecutive patients admitted to Spanish hospitals with laboratory-confirmed COVID-19 infection by real-time polymerase chain reaction (RT-PCR) assay for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) who showed clinical and analytical data suggestive of macrophage activation syndrome during admission until March 30, 2020 .
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sánchez-Barriga | Contact | +34 600162652 | maria.sanchezbarriga@juntadeandalucia.es |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Virgen Macarena | Recruiting | Seville | 41071 | Spain |
| Type | Date | Date Unknown |
|---|---|---|
| Release | Mar 17, 2021 | |
| Reset | Apr 1, 2021 | |
| Release | Sep 17, 2021 | |
| Reset | Sep 21, 2021 | |
| Release | May 6, 2022 | |
| Reset | Feb 3, 2023 |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Apr 7, 2020 | May 7, 2020 | Prot_SAP_000.pdf |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Mar 17, 2021 | Apr 1, 2021 | |||
| Sep 17, 2021 |
| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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| ID | Term |
|---|---|
| D007166 | Immunosuppressive Agents |
| ID | Term |
|---|---|
| D007155 | Immunologic Factors |
| D045505 | Physiological Effects of Drugs |
| D020228 | Pharmacologic Actions |
| D020164 | Chemical Actions and Uses |
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| Immunosuppressive |
| Drug |
Patients receiving immunosuppressive drugs (overall, and specific drugs) |
|
| Immunoglubulins | Drug | Patients receiving immunoglubulins |
|
| Secondary infections | Proportion of patients developing secondary infections | Up to 21 days |
| Digestive tract hemorrhage | Proportion of patients with digestive tract hemorrhage | Up to 21 days |
| Change in 7 points scale | Proportion of patients with imnprovement in 2 or more points in 7-point scale by WHO | Day 21 |
| Sep 21, 2021 |
| May 6, 2022 | Feb 3, 2023 |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |