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Effect of Treatments in Patients Hospitalized for Severe COVID-19 Pneumonia: a Multicenter Cohort Study

Effect of Treatments in Patients Hospitalized for Severe COVID-19 Pneumonia: a Multicenter Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04365764
Enrollment
400
Registered
2020-04-28
Start date
2020-03-14
Completion date
2022-12-31
Last updated
2023-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ARDS, Covid-19, Pneumonia

Brief summary

Several treatments have been used in during the Covid-19 pandemic of 2020. Using patients' registries from several hospitals in Paris, the investigators retrospectively analyzed associations between specific treatments, including but not limited to vaccines targeted against SARS-CoV-2, hydroxychloroquine, azithromycin, remdesivir, baricitinib, tocilizumab, sarilumab, lopinavir/ritonavir and oseltamivir; and clinical outcomes including, death and mechanical ventilation.

Detailed description

Several treatments have been used in during the Covid-19 pandemic of 2020. Using patients' registries from several hospitals in Paris, the investigators retrospectively analyzed associations between specific treatments, including but not limited to vaccines targeted against SARS-CoV-2, hydroxychloroquine, azithromycin, remdesivir, baricitinib, tocilizumab, sarilumab, lopinavir/ritonavir and oseltamivir; and clinical outcomes including, death and mechanical ventilation. Other outcomes of interest include: acute kidney injury, encephalopathy, need for intensive care unit transfers.

Interventions

None listed

Sponsors

Centre Hospitalier Intercommunal Robert Ballanger
CollaboratorOTHER
Centre Hospitalier Intercommunal Montfermeil-Le Raincy
CollaboratorUNKNOWN
CMC Ambroise Paré
CollaboratorOTHER
Groupe Hospitalier Pitie-Salpetriere
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* admitted for severe Covid-19 pneumonia (i.e. requiring O2-support more than 6L/min with SpO2\<96%)

Exclusion criteria

* patients who were previously in ICU * patients already hospitalized prior to study start date * patients in palliative care * lack of consent

Design outcomes

Primary

MeasureTime frameDescription
Composite of death and mechanical ventilation14-days follow-upComposite of death and mechanical ventilation (i.e. intubation)

Secondary

MeasureTime frameDescription
Death14-days follow-upDeath
Mechanical ventilation14-days follow-upEnabled by intubation
Composite of death and mechanical ventilation28-days follow-upComposite of death and mechanical ventilation
World Health Organization score14-days follow-upWorld Health Organization score

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026