Dexamethasone for COVID-19
Primary Purpose
Covid19
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Dexamethasone
Sponsored by

About this trial
This is an interventional treatment trial for Covid19 focused on measuring COVID 19
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years old
- RT-PCR confirmed COVID-19 infection
- Positive pressure ventilation (non-invasive or invasive) or high flow nasal cannula (HFNC) or need supplemental oxygen with oxygen mask or nasal cannula
Exclusion Criteria:
- Underlying disease requiring chronic corticosteroids
- Severe adverse events before admission, i.e. cardiac arrest;
- Contraindication for corticosteroids;
- Death is deemed to be imminent and inevitable during the next 24 hours
- Recruited in other clinical intervention trial
- Pregnancy
- Patient on judicial protection
Sites / Locations
- University of Oklahoma Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Dexamethasone 20 mg
Dexamethasone 6 mg
Arm Description
Dexamethasone 20 mg daily for 5 days, followed by dexamethasone 10 mg daily for 5 days
Dexamethasone 6 mg daily for 10 days
Outcomes
Primary Outcome Measures
World Health Organization ordinal scale at day 28
1. Not hospitalized, no limitations on activities 2. Not hospitalized, limitation on activities 3. Hospitalized, not requiring supplemental oxygen 4. Hospitalized, requiring supplemental oxygen by mask or nasal prongs 5. Hospitalized, on non-invasive ventilation or high flow oxygen devices 6. Hospitalized, on invasive mechanical ventilation 7. Hospitalized, on invasive mechanical ventilation + additional organ support (pressors, RRT, ECMO) 8. Death
Secondary Outcome Measures
Ventilator-free days
Days being alive and free from mechanical ventilation at day 28 after enrollment. For patients who die, it is 0.
28-day mortality
All-cause mortality at 28 days after enrollment
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04707534
Brief Title
Dexamethasone for COVID-19
Official Title
Effects of Higher Dose and Lower Dose of Dexamethasone for Hospitalized Patients With COVID-19
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
January 21, 2021 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
March 4, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oklahoma
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This open label clinical trial is to evaluate two different doses of dexamethasone on the health outcome using World Health Organization ordinal scale at day 28 in hospitalized patients with COVID-19.
Detailed Description
The coronavirus disease 2019 (COVID-19) pandemic is a serious global health threat. Multiple antiviral or immunomodulatory therapies have failed to show any mortality benefit for patients with COVID-19. Dexamethasone was shown in prior studies to improve mortality and ventilator free days. However, it is unclear what dose of dexamethasone is most beneficial in hospitalized patients with COVID-19. This randomized single center open label clinical trial is to evaluate two different doses of dexamethasone (20mg vs. 6mg) on the health outcome for hospitalized patients with COVID-19. The intervention arm is dexamethasone 20mg daily for 5 days, followed by dexamethasone 10mg daily for 5 days. The comparator is dexamethasone 6mg daily for 10 days. Three hundred participants will be enrolled. The primary outcome is clinical improvement using World Health Organization ordinal scale at day 28.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
COVID 19
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dexamethasone 20 mg
Arm Type
Experimental
Arm Description
Dexamethasone 20 mg daily for 5 days, followed by dexamethasone 10 mg daily for 5 days
Arm Title
Dexamethasone 6 mg
Arm Type
Active Comparator
Arm Description
Dexamethasone 6 mg daily for 10 days
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Dexamethasone
Primary Outcome Measure Information:
Title
World Health Organization ordinal scale at day 28
Description
1. Not hospitalized, no limitations on activities 2. Not hospitalized, limitation on activities 3. Hospitalized, not requiring supplemental oxygen 4. Hospitalized, requiring supplemental oxygen by mask or nasal prongs 5. Hospitalized, on non-invasive ventilation or high flow oxygen devices 6. Hospitalized, on invasive mechanical ventilation 7. Hospitalized, on invasive mechanical ventilation + additional organ support (pressors, RRT, ECMO) 8. Death
Time Frame
28 days from study enrollment
Secondary Outcome Measure Information:
Title
Ventilator-free days
Description
Days being alive and free from mechanical ventilation at day 28 after enrollment. For patients who die, it is 0.
Time Frame
28 days from study enrollment
Title
28-day mortality
Description
All-cause mortality at 28 days after enrollment
Time Frame
28 days from study enrollment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years old
RT-PCR confirmed COVID-19 infection
Positive pressure ventilation (non-invasive or invasive) or high flow nasal cannula (HFNC) or need supplemental oxygen with oxygen mask or nasal cannula
Exclusion Criteria:
Underlying disease requiring chronic corticosteroids
Severe adverse events before admission, i.e. cardiac arrest;
Contraindication for corticosteroids;
Death is deemed to be imminent and inevitable during the next 24 hours
Recruited in other clinical intervention trial
Pregnancy
Patient on judicial protection
Facility Information:
Facility Name
University of Oklahoma Medical Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
36190994
Citation
Wu H, Daouk S, Kebbe J, Chaudry F, Harper J, Brown B. Low-dose versus high-dose dexamethasone for hospitalized patients with COVID-19 pneumonia: A randomized clinical trial. PLoS One. 2022 Oct 3;17(10):e0275217. doi: 10.1371/journal.pone.0275217. eCollection 2022.
Results Reference
derived
Learn more about this trial
Dexamethasone for COVID-19
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