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| ID | Type | Description | Link |
|---|---|---|---|
| 2020-001553-48 | EudraCT Number |
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Competent Authority's decision
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Infection with the SARS-Cov-2 virus, responsible of severe acute respiratory distress syndrome (SARS), is an emerging infectious disease called Covid-19 and declared as pandemic by the World Health Organization on March 11, 2020. This pandemic is responsible of significant mortality. In France, several thousand patients are hospitalized in intensive care units, and their number continues to increase. Mortality during Covid-19 is mainly linked to acute respiratory distress syndrome, which frequency is estimated in France to occur in 6% of infected patients. Comorbidities such as cardiovascular conditions, obesity and diabetes increase susceptibility to severe forms of Covid-19 and associated mortality. Therapeutic management has three components: symptomatic management, including supplementary oxygen therapy and in case of respiratory distress mechanical ventilation; the antiviral approach; and immunomodulation, aiming at reducing inflammation associated with viral infection, which is considered to take part in severe presentations of the disease.
During Covid-19 viral pneumonia related to SARS-COv-2, there is a significant release of pro-inflammatory cytokines in the acute phase of viral infection, which could participate in viral pneumonia lesions. In children with less mature immune system than adults, SARS-Cov-2 infection is less severe. The current prevailing assumption is that severe forms of Covid-19 may not only be related to high viral replication, but also to an excessive inflammatory response favoring acute lung injury and stimulating infection.
The investigators hypothesize that early control of the excessive inflammatory response may help reducing the risk of acute respiratory distress syndrome.
The investigators will evaluate the benefit, safety and tolerability of corticosteroid therapy to reduce the rate of subjects hospitalized for Covid-19 viral pneumonia who experience clinical worsening with a need of high-flow supplemental oxygen supplementation or transfer in intensive care units for respiratory support.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prednisone group | Experimental | Prednisone during 10 days after randomization |
|
| Control group | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Prednisone | Drug | The experimental group will receive oral prednisone during 10 days (0.75 mg/kg/day during 5 days then 20 mg/day during 5 more days) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients with a theoretical respiratory indication for transfer to intensive care unit evaluated by a SpO2 <90% stabilized at rest and under not more than 5 L / min of supplemental oxygen using medium concentration mask. | SpO2 <90% stabilized at rest and under not more than 5 L / min of supplemental oxygen using medium concentration mask. measured twice at 5-15 min intervalsThe average value of the two measurements will be calculated. | 7 days |
| Measure | Description | Time Frame |
|---|---|---|
| disease severity assessed on a 7-level ordinal scale | level1: not hospitalized no limited activities, level 7: death | 7 days |
| number of patients with a supplemental oxygen use | 7 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jean-François MORNEX | Hospices Civils de Lyon | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital Pneumologique et Cardiovasculaire Louis Pradel | Bron | France | ||||
| CH Annecy-Genevois |
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| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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| ID | Term |
|---|---|
| D011241 | Prednisone |
| D035061 | Control Groups |
| ID | Term |
|---|---|
| D011244 | Pregnadienediols |
| D011245 | Pregnadienes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 |
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| Control group | Other | The control group will receive standard of care according to the international recommendations and practices of the investigational site. No corticosteroid therapy can be prescribed in this group. |
|
| radiological signs on chest imaging | Reduction of radiological signs on chest imaging | 7 days |
| number of patients transferred to intensive care unit | 21 days |
| number of patients requiring invasive ventilation | 21 days |
| Duration of oxygen therapy | duration on days | 21 days |
| number of adverse events induced by corticosteroid treatment | 21 days |
| number of patients with infections other than SARS-CoV-2 | 21 days |
| number of deaths | 21 days |
| Épagny |
| France |
| Groupement Hospitalier Nord | Lyon | France |
| Hôpital Edouard Herriot | Lyon | France |
| Hôpital St Joseph Saint Luc | Lyon | France |
| Hôpital St Joseph | Marseille | France |
| Centre hospitalier Lyon Sud | Pierre-Bénite | France |
| CHU St Etienne | Saint-Etienne | France |
| Clinique Charcot | Sainte-Foy-lès-Lyon | France |
| Clinique des Portes du Sud | Vénissieux | France |
| CHG Vienne | Vienne | France |
| Médipôle | Villeurbanne | France |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
| D015340 | Epidemiologic Research Design |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D012107 | Research Design |
| D008722 | Methods |