Effect of Corticosteroid Treatment on Prognosis in ARDS Secondary to Covid-19

NCT ID: NCT04586114

Last Updated: 2020-10-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-03-01

Study Completion Date

2020-12-31

Brief Summary

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Study conducted on hospitalized patient in critical ill units in Nancy and Metz to evaluate if early corticosteroid treatment in first seven days after admission improve patients outcome in Acute Respiratory Distress Syndrome secondary to Covid-19 compared to later corticosteroid therapy or no treatment. Also comparison of acquired infection with or without corticosteroid treatment during hospitalisation.

Detailed Description

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Conditions

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Acute Respiratory Distress Syndrome Secondary to Covid-19

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Early corticosteroid

Corticosteroid treatment within first seven days after ICU admission

Corticosteroids and Derivatives

Intervention Type DRUG

Any systemic corticosteroid treatment administrated during ICU stay

Late corticosteroid

Corticosteroid treatment later than seventh day's after ICU admission

Corticosteroids and Derivatives

Intervention Type DRUG

Any systemic corticosteroid treatment administrated during ICU stay

No corticosteroid

No corticosteroid treatment during ICU stay

No interventions assigned to this group

Interventions

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Corticosteroids and Derivatives

Any systemic corticosteroid treatment administrated during ICU stay

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* ICU hospitalized with acute respiratory distress syndrome secondary to Sars-Cov-2 infection diagnosed by PCR test
* Hospitalized from 01/03/2020 to 30/04/2020

Exclusion Criteria

* Mechanical ventilation more than 48 hours at admission
* Transfert to another ICU during stay for bed management
* Corticosteroid treatment at admission
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sebastien GIBOT

Role: PRINCIPAL_INVESTIGATOR

Central Hospital, Nancy, France

Locations

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Hopital Central, Service de Reanimation Medicale

Nancy, , France

Site Status

Countries

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France

Other Identifiers

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2020PI109

Identifier Type: -

Identifier Source: org_study_id

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