The aim of the study is to evaluate two differents regimens of corticosteroids (prednisolone versus dexamethasone) on D28 mortality in patients with CoViD 19 pneumonia requiring oxygen supplementation
Low-dose glucocorticoid treatment is the only medication showing a significant reduction in mortality in cases of COVID-19 pneumonia requiring oxygen supplementation or ventilatory support. Intravenous or oral dexamethasone are well evaluated in randomized study but other oral corticosteroids are not. Compared to dexamethasone, prednisolone is more available in France and easily taken by patients, especially in case of home medical care. The pharmacokinetics/pharmacodynamics of prednisolone and dexamethasone are different. To obtain similar effects, prednisolone should be theoretically taken twice a day and at a superior dose than the strict prednisone equivalence of 6mg dexamethasone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
89
Patients will take 60 mg per day of Prednisolone (40 mg morning and 20 md evening) between D1 to D10
Patients will take 60 mg per day of Prednisolone (40 mg morning and 20 md evening) between D1 to D10
Department of Emergency, Hospital Victor Dupouy
Argenteuil, France
Department of Pneumology and Infectious Medicine, Hospital Carnelle Portes de l'Oise
Beaumont, France
Department of Infectious and Tropical Diseases, Hospital Simone Veil
Eaubonne, France
Mortality assessment at D28
Assessment of vital status at D28 in Dexamethason arms vs Prednisolone arms
Time frame: At Day 28
Assessment of clinical course in both groups (arms)
The clinical course for each patient will be measured, for several items, and compared between both groups to see if a significant difference is observed. Items, considered for comparison, are listed below : * Number of oxygen therapy days, * Number of patients requiring oxygen therapy increase (High-Flow Oxygen Therapy, CPAP/BIPAP, mechanical ventilation, ECMO) * Number of hospital days * Number of patient admitted in Resuscitation Unit /Intensive care Unit * Number of patient with organic damage other than lung * Number of disease-related infection other than SARS-Cov-2 * Frequency and evolution of complication of corticosteroid therapy (Severity evaluated according to CTCAE (diabetes, acute psychosis or other adverse effect consider to be link to corticosteroide therapy by investigator))
Time frame: At Day 28
Measurement of evolution of respiratory symptoms in both groups (arms)
Evolution of respiratory symptoms will be measured for each patient, for several items, and compared between both groups to see if a significant difference is observed. Items, considered for comparison, are listed below : * Oxygen saturation rate, * Oxygen flow, * Respiratory rate
Time frame: From Day 0 to Day 28
Assessment of patient satisfaction towards the treatment
Assessment of patient satisfaction with a satisfaction questionnaire (Likert-type scale) For each item, patient ticks : Very satisfied, Satisfied, Unsatisfied or Very unsatisfied
Time frame: At Day 28
Comparison betwween D1 and D28 of patient quality of life evolution between randomization groups (arms)
Measurement of patient quality of life evolution with EQ5D self-assessment questionnaire at day1 and day 28. For item of mobility, autonomy and current activities, patient ticks : I have no problem, I have some problems or I am I am unable to do For item of pain and anxiety/depression, patient ticks : no, moderate or severe
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Department of Infectious Medicine, Hospital of Gonesse
Gonesse, France
Department of Internal Medicine, Hospital Emile Roux - Le Puy-en-Velay
Le Puy-en-Velay, France
Department of Infectious and Tropical Diseases, Hospital René Dubos,
Pontoise, France
Department of Infectious and respiratory Diseases, Hospital Delafontaine
Saint-Denis, France
Department of Pneumology and Infectious Diseases, Hospital of Saint-Quentin
Saint-Quentin, France
Time frame: At Day 1 and Day 28
Comparison betwween D1 and D28 of adverse events and adverse effects between randomization groups (arms)
Measurement of adverse events number and adverse effects number during the 28 days of the study
Time frame: At Day 28