Dexamethasone and Oxygen Support Strategies in ICU Patients With Covid-19 Pneumonia (COVIDICUS)
Primary Purpose
Acute Hypoxemic Respiratory Failure, COVID-19
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Dexamethasone injection
placebo
conventional oxygen
CPAP
HFNO
mechanical ventilation
Sponsored by
About this trial
This is an interventional treatment trial for Acute Hypoxemic Respiratory Failure focused on measuring COVID-19, acute hypoxemic respiratory failure (AHRF)
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Admitted to ICU within 48 hours
- Confirmed or highly suspected COVID-19 infection
- Acute hypoxemic respiratory failure (PaO2 <70 mmHg or SpO2<90% on room air or tachypnea>30/min or labored breathing or respiratory distress; need for oxygen flow >=6L/min)
- Any treatment intended to treat the SARS-CoV-2 infection in the absence of contraindications (either as a compassionate use or in the context of a clinical trial, i.e remdesivir, lopinavir/ritonavir, favipiravir, hydroxychloroquine and any other new drug with potential activity).
Non-inclusion Criteria:
- Moribund status
- Pregnancy or breastfeeding
- Long term corticotherapy at a dose of 0.5mg/kg/j or higher
- Active and untreated bacterial, fungal or parasitic infection
- Not Written informed consent from the patient or a legal representative if appropriate . If absence a legal representative the patient may be included in emergency procedure
- hypersensitivity to dexamethasone or to any of the excipients
- Not Affiliation to the French social security
Sites / Locations
- Hopital Bichat - Aphp
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Experimental
Experimental
Placebo Comparator
Experimental
Arm Label
Standard oxygen 1
Standard oxygen 2
CPAP 1
CPAP 2
HFNO 1
HFNO 2
mechanically ventilated 1
mechanically ventilated 2
Arm Description
Standard oxygen and placebo of Dexamethasone
Standard oxygen and Dexamethasone
CPAP and placebo of Dexamethasone
CPAP and Dexamethasone
HFNO and placebo of Dexamethasone
HFNO and Dexamethasone
placebo
Dexamethasone
Outcomes
Primary Outcome Measures
The time-to-death from all causes
The time-to-death from all causes within the first 60 days after randomization.
The time to need for mechanical ventilation (MV)
the time to need for mechanical ventilation (MV), as defined by any of the 3 criteria for intubation within the first 28 days after randomization.
Secondary Outcome Measures
The viral load in the respiratory tract
The cycle threshold for SARS-CoV-2 PCR at baseline, day 7+/-1 and day 10 +/- in samples of the same origin (preferably subglottic i.e. bronchoalveolar lavage or tracheal aspiration, otherwise nasopharyngeal swab)
Number of patient with at least one episode of healthcare-associated infections
Proportion of patients with at least one episode of any healthcare-associated infection between randomization and D28
Number of days alive without mechanical ventilation
To compare the exposition to mechanical ventilation
Measure of SOFA score
Changes in SOFA (Sepsis-related Organ Failure Assessment) score. (min = 0 for normal status max = 24 for worse status)
Number of days alive without renal replacement therapy
to compare the exposition to renal replacement therapy
Lengths of ICU-stay
To compare the lengths of ICU
Lengths of hospital-stay
To compare the lengths of hospital-stay
Number of patients with severe hypoxemia,
Proportion of patients with severe hypoxemia, which is defined as an oxygen saturation of less than 80% during the same interval during the interval between induction and 2 minutes after tracheal intubation
Proportion of patients with cardiac arrest within 1 hour after intubation
Proportion of patients with cardiac arrest within 1 hour after intubation
Overall survival
To compare Overall survival after randomization
Full Information
NCT ID
NCT04344730
First Posted
April 9, 2020
Last Updated
February 6, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT04344730
Brief Title
Dexamethasone and Oxygen Support Strategies in ICU Patients With Covid-19 Pneumonia
Acronym
COVIDICUS
Official Title
Dexamethasone and Oxygen Support Strategies in ICU Patients With Covid-19 pneumonia_COVIDICUS
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 10, 2020 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The main manifestation of COVID-19 is acute hypoxemic respiratory failure (AHRF). In patients with AHRF, the need for invasive mechanical ventilation is associated with high mortality.
Two hypotheses will be tested in this study. The first hypothesis is the benefit of corticosteroid therapy on severe COVID-19 infection admitted in ICU in terms of survival.
The second hypothesis is that, in the subset of patients free of mechanical ventilation at admission, either Continuous Positive Airway Pressure (CPAP) or High-Flow Nasal Oxygen (HFNO) allows to reduce intubation rate safely during COVID-19 related acute hypoxemic respiratory failure.
Detailed Description
The main manifestation of COVID-19 is acute hypoxemic respiratory failure (AHRF). In patients with AHRF, the need for invasive mechanical ventilation is associated with high mortality.
Two hypotheses will be tested in this study. The first hypothesis is the benefit of corticosteroid therapy on severe COVID-19 infection admitted in ICU in terms of survival.
The second hypothesis is that, in the subset of patients free of mechanical ventilation at admission, either Continuous Positive Airway Pressure (CPAP) or High-Flow Nasal Oxygen (HFNO) allows to reduce intubation rate safely during COVID-19 related acute hypoxemic respiratory failure.
The main objective is to assess the impact of dexamethasone on overall mortality at day-60 after randomization in patients admitted in ICU for severe COVID-19 infection.
In non mechanical ventilation (MV) patients, the additional objective is to assess whether oxygen support based on either HFNO or CPAP modality in COVID-19 related AHRF reduces the need for mechanical ventilation at day-28.
An ancillary study CACAO (COVIDICUS air contamination) will be performed in 4 centers aiming at assessing the environmental contamination by SARS-CoV-2 according to the oxygen support modality. Additional funding will be searched for these analyses (submitted for ANR call).
A metanalysis on individual data will be performed using patients enrolled in the 3 PHRC flash exploring the activity of corticosteroids.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Hypoxemic Respiratory Failure, COVID-19
Keywords
COVID-19, acute hypoxemic respiratory failure (AHRF)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
In non-mechanically ventilated patients, a 2x2 factorial design will be used to assess the two interventions, separately.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The masking label is available only for the treatment assignation
Allocation
Randomized
Enrollment
550 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard oxygen 1
Arm Type
Placebo Comparator
Arm Description
Standard oxygen and placebo of Dexamethasone
Arm Title
Standard oxygen 2
Arm Type
Experimental
Arm Description
Standard oxygen and Dexamethasone
Arm Title
CPAP 1
Arm Type
Experimental
Arm Description
CPAP and placebo of Dexamethasone
Arm Title
CPAP 2
Arm Type
Experimental
Arm Description
CPAP and Dexamethasone
Arm Title
HFNO 1
Arm Type
Experimental
Arm Description
HFNO and placebo of Dexamethasone
Arm Title
HFNO 2
Arm Type
Experimental
Arm Description
HFNO and Dexamethasone
Arm Title
mechanically ventilated 1
Arm Type
Placebo Comparator
Arm Description
placebo
Arm Title
mechanically ventilated 2
Arm Type
Experimental
Arm Description
Dexamethasone
Intervention Type
Drug
Intervention Name(s)
Dexamethasone injection
Other Intervention Name(s)
experimental treatment
Intervention Description
Box of 10 DEXAMETHASONE 20 mg / 5 ml, solution for injection in ampoule of 5mL. Each allocated box contains complete treatment from D1 to D10 for one patient.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Box of 10 NaCl 0,9% , solution for injection in ampoule of 5mL. Each allocated box contains complete treatment from D1 to D10 for one patient.
Intervention Type
Procedure
Intervention Name(s)
conventional oxygen
Intervention Description
The oxygen flow will be adjusted to maintain an oxygen saturation level of 92% or more, as measured by means of pulse oximetry (SpO2)
Intervention Type
Procedure
Intervention Name(s)
CPAP
Intervention Description
Patients assigned to the CPAP plus oxygen group will receive periods of CPAP in addition to the standard treatment.The oxygen flow will be adjusted to maintain an oxygen saturation level of 92% or more, as measured by means of pulse oximetry (SpO2)
Intervention Type
Procedure
Intervention Name(s)
HFNO
Intervention Description
TIn the high-flow-nasal cannula group, oxygen will be delivered through a heated humidifier (Airvo-2, Fisher and Paykel Healthcare) and applied continuously through large-bore binasal prongs, with a gas flow rate of 30 liters per minute and adjusted based on the clinical response. FiO2 will be adjusted for the target SpO2
Intervention Type
Procedure
Intervention Name(s)
mechanical ventilation
Intervention Description
The oxygen flow will be adjusted to maintain an oxygen saturation level of 92% or more, as measured by means of pulse oximetry (SpO2)
Primary Outcome Measure Information:
Title
The time-to-death from all causes
Description
The time-to-death from all causes within the first 60 days after randomization.
Time Frame
day-60
Title
The time to need for mechanical ventilation (MV)
Description
the time to need for mechanical ventilation (MV), as defined by any of the 3 criteria for intubation within the first 28 days after randomization.
Time Frame
day-28.
Secondary Outcome Measure Information:
Title
The viral load in the respiratory tract
Description
The cycle threshold for SARS-CoV-2 PCR at baseline, day 7+/-1 and day 10 +/- in samples of the same origin (preferably subglottic i.e. bronchoalveolar lavage or tracheal aspiration, otherwise nasopharyngeal swab)
Time Frame
day-10
Title
Number of patient with at least one episode of healthcare-associated infections
Description
Proportion of patients with at least one episode of any healthcare-associated infection between randomization and D28
Time Frame
day-28
Title
Number of days alive without mechanical ventilation
Description
To compare the exposition to mechanical ventilation
Time Frame
day-28
Title
Measure of SOFA score
Description
Changes in SOFA (Sepsis-related Organ Failure Assessment) score. (min = 0 for normal status max = 24 for worse status)
Time Frame
day-1 to day 3, day 7, day 10, day 21, day 28
Title
Number of days alive without renal replacement therapy
Description
to compare the exposition to renal replacement therapy
Time Frame
day-28
Title
Lengths of ICU-stay
Description
To compare the lengths of ICU
Time Frame
day-60
Title
Lengths of hospital-stay
Description
To compare the lengths of hospital-stay
Time Frame
day-60
Title
Number of patients with severe hypoxemia,
Description
Proportion of patients with severe hypoxemia, which is defined as an oxygen saturation of less than 80% during the same interval during the interval between induction and 2 minutes after tracheal intubation
Time Frame
day 60
Title
Proportion of patients with cardiac arrest within 1 hour after intubation
Description
Proportion of patients with cardiac arrest within 1 hour after intubation
Time Frame
day 60
Title
Overall survival
Description
To compare Overall survival after randomization
Time Frame
day 60
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Admitted to ICU within 48 hours
Confirmed or highly suspected COVID-19 infection
Acute hypoxemic respiratory failure (PaO2 <70 mmHg or SpO2<90% on room air or tachypnea>30/min or labored breathing or respiratory distress; need for oxygen flow >=6L/min)
Any treatment intended to treat the SARS-CoV-2 infection in the absence of contraindications (either as a compassionate use or in the context of a clinical trial, i.e remdesivir, lopinavir/ritonavir, favipiravir, hydroxychloroquine and any other new drug with potential activity).
Non-inclusion Criteria:
Moribund status
Pregnancy or breastfeeding
Long term corticotherapy at a dose of 0.5mg/kg/j or higher
Active and untreated bacterial, fungal or parasitic infection
Not Written informed consent from the patient or a legal representative if appropriate . If absence a legal representative the patient may be included in emergency procedure
hypersensitivity to dexamethasone or to any of the excipients
Not Affiliation to the French social security
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean François TIMSIT, Pr
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital Bichat - Aphp
City
Paris
ZIP/Postal Code
75018
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
35788622
Citation
Bouadma L, Mekontso-Dessap A, Burdet C, Merdji H, Poissy J, Dupuis C, Guitton C, Schwebel C, Cohen Y, Bruel C, Marzouk M, Geri G, Cerf C, Megarbane B, Garcon P, Kipnis E, Visseaux B, Beldjoudi N, Chevret S, Timsit JF; COVIDICUS Study Group. High-Dose Dexamethasone and Oxygen Support Strategies in Intensive Care Unit Patients With Severe COVID-19 Acute Hypoxemic Respiratory Failure: The COVIDICUS Randomized Clinical Trial. JAMA Intern Med. 2022 Sep 1;182(9):906-916. doi: 10.1001/jamainternmed.2022.2168.
Results Reference
derived
Learn more about this trial
Dexamethasone and Oxygen Support Strategies in ICU Patients With Covid-19 Pneumonia
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