Selenium as a Potential Treatment for Moderately-ill, Severely-ill, and Critically-ill COVID-19 Patients. (SeCOVID)
Covid19

About this trial
This is an interventional treatment trial for Covid19 focused on measuring COVID-19 Pneumonia, Cytokine Storm, ARDS, Moderate COVID-19 Infections, Severe COVID-19 Infections, Critical COVID-19 Infections, Selenium
Eligibility Criteria
Inclusion Criteria:
- Willing and able to provide written informed consent, or with a legal representative who can provide informed consent, or enrolled under International Conference on Harmonization (ICH) E6(R2) 4.8.15 emergency use provisions as deemed necessary by the investigator (age ≥18) prior to performing study procedure.
- Aged ≥ 18 years.
- Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV)-2 infection confirmed by polymerase chain reaction (PCR) test ≤ 4 days before randomization.
- Currently hospitalized.
- Peripheral capillary oxygen saturation (SpO2) ≤ 94% or requiring supplemental oxygen on screening.
Exclusion Criteria:
- Participation in any other clinical trial of an experimental treatment for COVID-19.
- Evidence of multiorgan failure.
- Mechanically ventilated for > 5 days.
- Alanine Aminotransferase (ALT) or aspartate aminotransferase (AST) > 5 X upper limit of normal (ULN).
- Creatinine clearance < 50 mL/min.
Sites / Locations
- CHRISTUS Good Shepherd Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Selenious Acid + Standard Of Care (SOC)
Standard Of Care (SOC) + Placebo
Participants who are moderately-ill, severely-ill, or critically ill will receive a Selenious Acid infusion of 2000µg on day 1 as a loading dose infusion, followed by a continuous infusion of Selenious Acid at a maintenance dose of 1000µg daily on days 2-14 together with continued Standard Of Care therapy.
Participants will receive a Saline-based placebo infusion of 2000µg on day 1 as a loading dose, followed by continuous infusion of a Saline-based placebo at a maintenance dose of 1000µg daily on days 2-14. Standard Of Care is to be determined according to patients' clinical picture and may include Dexamethasone, Azithromycin, Ceftriaxone, Remdesivir, Convalescent Plasma.