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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04359511
Other study ID # CORTI-COVID-19-HUGO
Secondary ID DR200136
Status Withdrawn
Phase Phase 3
First received
Last updated
Start date July 3, 2020
Est. completion date July 3, 2020

Study information

Verified date May 2021
Source University Hospital, Tours
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To date, there is no efficient therapeutics to prevent or treat COVID-19 related pulmonary failure. Corticosteroids (CS) could be a helpful therapeutic. Retrospective reports suggested survival improvement in patients with acute respiratory distress syndrome (ARDS). CT scan for COVID19 hospitalized patients showed sometimes unusual aspects of pneumonia, suggestive of an organizing phase of diffuse alveolar damage (DAD). We hypothesize that, in the context of alveolar aggression induced by COVID-19, CT scan could help to individualize patients with a high probability of pulmonary organizing process who could benefit from CS treatment.


Description:

"Severe acute respiratory syndrome" coronavirus 2 (SARS-Cov-2) is a new coronavirus that induces pneumonia called Corona Virus Disease- 19 (COVID-19), an infected 1.5 million people worldwide and caused the more than 85,000 patients died. COVID-19 usually comes in the form of viral pneumonia but with the peculiarities of a risk frequent worsening towards acute respiratory distress syndrome (ARDS) and a usual duration of oxygen dependence in fragile patients by their age or their comorbidities. To date, there is no therapy effective in preventing or treating COVID-19. Drug identification is a major concern and a public health emergency. Retrospective study (Wu 2020) highlighted improved survival in COVID-19 patients with acute ARDS and treated with corticosteroids (CS). So even in the absence of evidence of effectiveness, the SCs are used for COVID-19 oxygen-dependent patients or with an ARDS. However, their benefit / risk remains debated (Russel 2020). On histological samples of COVID-19, diffuse alveolar damage (DAD) has been especially observed (Hanley 2020). DAD is described histologically in an exudative phase, an organizational phase and a irreversible fibrotic phase (Hughes 2017). SC could have an effect beneficial by limiting the exudative / inflammatory phase but also that organization whose histological and CT aspects are sometimes indistinguishable from organized pneumonia, a form of pulmonary repair aberrant very corticosensitive (Travis 2013). Chest scans performed in the face of the persistence or worsening of oxygen dependence beyond the 7th day of COVID-19 symptoms, could help discern indirect complications (pulmonary embolism, exacerbation of COPD, bacterial superinfection, etc.) of an unfavorable course COVID-19 (by displaying an aspect suggesting DAD in particular during the organization phase). We hypothesize that, in the context of COVID-19, the SCs may be beneficial in patients with CT scans thoracic images suggestive of DAD either at the exudative phase or at the pulmonary organization phase.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 3, 2020
Est. primary completion date July 3, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients = 18 years old, - Hospitalized with a proven diagnosis of COVID-19 (SARS-CoV-2 positive in RTPCR), in medicine or in intensive care. - With a need for oxygen therapy = 2 l / min to maintain a Sp02> 92% or a need for oxygen therapy to maintain a PaO2 / FiO2> 300 mmHg (for intubated patients). - With a chest scanner at least 7 days after the onset of symptoms, and whose centralized interpretation shows a CT scan aspect suggestive of intense and predominant DAD which can explain the patient's oxygen dependence. - Signature of a free, written and informed consent by the patient, or the person of trust - Affiliate or beneficiary of a social security scheme. Exclusion Criteria: - Patients already treated by CS for a chronic disease. - Patients with a known contraindication to SC, such as hypersensitivity. - Patients at risk of dying within 48 hours. - Pregnant or breastfeeding women. - Patients under guardianship, curatorship, safeguard of justice. - Poor understanding of the French language.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Prednisone
prednisone 0.7 mg/kg/d (PO)
Hydrocortisone
hémisuccinate d'hydrocortisone 3,5 mg/kg/jour (IV)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Tours

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical improvement defined by the improvement of 2 points on a 7-category ordinal scale, at 14 days. The 7-category ordinal scale is as follow:
Not hospitalized with resumption of usual activities
Not hospitalized, but unable to resume usual activities
Hospitalized, not requiring O2
Hospitalized, requiring O2 from 1 to 5 l/min
Hospitalized, requiring O2 >6 l/min, nasal high-flow O2, non-invasive mechanical ventilation, or both
Hospitalized, requiring ECMO, invasive mechanical ventilation, or both
Death.
14 days
Secondary Proportion of patients free of oxygen at day 14 and 28 14 and 28 days
Secondary Proportion of patients discharged alive from hospital at day 14 and 28 14 and 28 days
Secondary Time to discharge for patients alive 28 days
Secondary Proportion of patients that were hospitalized to ICU or who died at day 14 and 28 14 and 28 days
Secondary 14 and 28 day mortality rate 14 and 28 days
Secondary The time until weaning from oxygen therapy 28 days
Secondary The proportion of patients with clinical degradation of at least 1 point on the ordinal scale to 7 categories on D14 and D28 14 and 28 days
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