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Dexamethasone for COVID-19 Related ARDS: a Multicenter, Randomized Clinical Trial

Primary Purpose

Respiratory Distress Syndrome, Adult, Covid-19

Status
Terminated
Phase
Phase 3
Locations
Argentina
Study Type
Interventional
Intervention
High-Dose Dexamethasone
Sponsored by
Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Distress Syndrome, Adult

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ARDS according to Berlin's definition
  • PCR confirmed COVID-19
  • Length of mechanical ventilation less or equal to 72 hours

Exclusion Criteria:

  • Pregnancy or breast-feeding women
  • Terminal illness with very poor prognosis according to the investigator judgement
  • Therapeutic limitation
  • Known immunocompromised condition
  • Chronic use of systemic corticosteroids
  • Participation in another randomized crinical trial
  • More than 5 days of treatment of low dose dexamethasone for COVID-19
  • Abscence of informed consent
  • Active participation in other randomized clinical trial

Sites / Locations

  • Hospital Universitario Sede Saaveda - IUC CEMIC
  • Hospital Universitario Sede Pombo - IUC CEMIC
  • Sanatorio Sagrado Corazon
  • Clínica Bazterrica

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

High dose Dexamethasone

Usual care - low dose Dexamethasone

Arm Description

Intravenous Dexamethasone 16 mg qd from day 1 to 5 followed by 8 mg qd from day 6 to 10

Intravenous Dexamethasone 6 mg qd for 10 days based on RECOVERY trial

Outcomes

Primary Outcome Measures

Ventilator-free days at 28 days
Days without ventilator support in the first 28 days following randomization
Time to successful discontinuation from mechanical ventilation
Time to event (successful discontinuation from mechanical ventilation)

Secondary Outcome Measures

28-days mortality
Dead rate within 28 days of randomization
Rate of nosocomial infections
Rate of ventilator associated pneumonia, blood stream infection, urinary tract infection or candidemia in the first 28 days following randomization
SOFA variation
Variation in SOFA over the first 10 days after randomization
Use of prone position
Cumulative hours spent on prone position
Delirium
Frequency of delirium at ICU discharge
Muscle weakness
mMRC score at ICU discharge
90-day mortality
Death rate within 90 days of randomization
Peak daily blood glucose
Interaction between treatment and daily change in glucose

Full Information

First Posted
May 16, 2020
Last Updated
May 28, 2021
Sponsor
Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
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1. Study Identification

Unique Protocol Identification Number
NCT04395105
Brief Title
Dexamethasone for COVID-19 Related ARDS: a Multicenter, Randomized Clinical Trial
Official Title
High Versus Low Dose Dexamethasone for the Treatment of COVID-19 Related ARDS: a Multicenter and Randomized Open-label Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
Low rate of recruitment
Study Start Date
May 21, 2020 (Actual)
Primary Completion Date
April 5, 2021 (Actual)
Study Completion Date
May 21, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
There is compelling data indicating that there is an excessive inflammatory response in some patients with COVID-19 leading them to develop ARDS that can be severe with a very poor prognosis. Many of these patients require very long mechanical ventilation times to survive, which have led to the collapse of the health system in some regions of the world. The current evidence for the treatment of these severe forms is inconsistent and most scientific societies and governmental or international organizations recommend evaluating treatments with randomized clinical trials. Corticosteroids, being non-specific anti-inflammatory drugs, could shorten the duration of respiratory failure and improve the prognosis. Due to the lack of solid data available regarding this serious disease, our objective is to randomly evaluate the efficacy and safety of the use of dexamethasone, a parenteral corticosteroid approved in Argentina, in patients with ARDS with confirmed respiratory infection due to SARS-CoV-2 (COVID-19). After RECOVERY trial prepublication, low dose (6 mg QD for 10 days) dexamethasone was recommended as the usual care treatment for severe COVID-19. At this time only 3 patients had been included in the trial. Thus, we updated our recommendations for centers and decided to compare two different doses of this glucocorticoid for the treatment of ADRS due to COVID-19.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress Syndrome, Adult, Covid-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High dose Dexamethasone
Arm Type
Experimental
Arm Description
Intravenous Dexamethasone 16 mg qd from day 1 to 5 followed by 8 mg qd from day 6 to 10
Arm Title
Usual care - low dose Dexamethasone
Arm Type
No Intervention
Arm Description
Intravenous Dexamethasone 6 mg qd for 10 days based on RECOVERY trial
Intervention Type
Drug
Intervention Name(s)
High-Dose Dexamethasone
Other Intervention Name(s)
Corticosteroid
Intervention Description
IV Dexamethasone administered once daily: 16 mg from day 1 to 5 and 8 mg from day 6 to 10
Primary Outcome Measure Information:
Title
Ventilator-free days at 28 days
Description
Days without ventilator support in the first 28 days following randomization
Time Frame
28 days after randomization
Title
Time to successful discontinuation from mechanical ventilation
Description
Time to event (successful discontinuation from mechanical ventilation)
Time Frame
28 days after randomization
Secondary Outcome Measure Information:
Title
28-days mortality
Description
Dead rate within 28 days of randomization
Time Frame
28 days after randomization
Title
Rate of nosocomial infections
Description
Rate of ventilator associated pneumonia, blood stream infection, urinary tract infection or candidemia in the first 28 days following randomization
Time Frame
28 days after randomization
Title
SOFA variation
Description
Variation in SOFA over the first 10 days after randomization
Time Frame
10 days after randomization
Title
Use of prone position
Description
Cumulative hours spent on prone position
Time Frame
10 days after randomization
Title
Delirium
Description
Frequency of delirium at ICU discharge
Time Frame
28 days after randomization
Title
Muscle weakness
Description
mMRC score at ICU discharge
Time Frame
28 days after randomization
Title
90-day mortality
Description
Death rate within 90 days of randomization
Time Frame
90 days after randomization
Title
Peak daily blood glucose
Description
Interaction between treatment and daily change in glucose
Time Frame
10 days after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ARDS according to Berlin's definition PCR confirmed COVID-19 Length of mechanical ventilation less or equal to 72 hours Exclusion Criteria: Pregnancy or breast-feeding women Terminal illness with very poor prognosis according to the investigator judgement Therapeutic limitation Known immunocompromised condition Chronic use of systemic corticosteroids Participation in another randomized crinical trial More than 5 days of treatment of low dose dexamethasone for COVID-19 Abscence of informed consent Active participation in other randomized clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pablo O Rodriguez, MD
Organizational Affiliation
Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Luis P Maskin, MD
Organizational Affiliation
Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Sede Saaveda - IUC CEMIC
City
Caba
ZIP/Postal Code
1431
Country
Argentina
Facility Name
Hospital Universitario Sede Pombo - IUC CEMIC
City
Ciudad Autonoma de Buenos Aires
ZIP/Postal Code
1425
Country
Argentina
Facility Name
Sanatorio Sagrado Corazon
City
Ciudad Autonoma de Buenos Aires
Country
Argentina
Facility Name
Clínica Bazterrica
City
Ciudad Autónoma de Buenos Aires
ZIP/Postal Code
1425
Country
Argentina

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32843098
Citation
Maskin LP, Olarte GL, Palizas F Jr, Velo AE, Lurbet MF, Bonelli I, Baredes ND, Rodriguez PO. High dose dexamethasone treatment for Acute Respiratory Distress Syndrome secondary to COVID-19: a structured summary of a study protocol for a randomised controlled trial. Trials. 2020 Aug 26;21(1):743. doi: 10.1186/s13063-020-04646-y.
Results Reference
derived
Links:
URL
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447582
Description
Protocol publication

Learn more about this trial

Dexamethasone for COVID-19 Related ARDS: a Multicenter, Randomized Clinical Trial

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