Study Results
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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COMPLETED
50 participants
OBSERVATIONAL
2020-04-01
2020-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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SARS-CoV2 patients that received dexamethasone
Dexamethasone
4mg dexamethasone was given to some patients three times daily for 2 days, 2 times daily for 2 days, once daily for 2 days.
Interventions
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Dexamethasone
4mg dexamethasone was given to some patients three times daily for 2 days, 2 times daily for 2 days, once daily for 2 days.
Eligibility Criteria
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Inclusion Criteria
2. All patients with severe disease with evidence of escalating oxygen requirements
3. The presence of secondary bacterial infections as a probable cause of increasing CRP levels was excluded in all selected patients.
4. Pulmonary embolism and /or cardiac dysfunction were excluded as probable causes of worsening hypoxia in all selected patients.
Exclusion Criteria
2. Patient with associated COPD exacerbation who would benefit from the use of steroids.
3. Patients with Diabetic ketoacidosis, hyperglycemic hyperosmolar state, active concurrent bacterial infections.
4. Patients with history of steroid-induced mania and/or psychosis.
18 Years
ALL
Yes
Sponsors
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The Miriam Hospital
OTHER
Responsible Party
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Principal Investigators
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Kwame Dapaah-Afriyie, MD
Role: PRINCIPAL_INVESTIGATOR
The Miriam Hospital
Locations
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The Miriam Hospital
Providence, Rhode Island, United States
Countries
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Other Identifiers
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20-027
Identifier Type: -
Identifier Source: org_study_id
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