This is a Phase II interventional study will test the efficacy of quintuple therapy (Hydroxychloroquine, Azithromycin, Vitamin C, Vitamin D, and Zinc) in the treatment of patients with COVID-19 infection).
In this study patients will be treated with a combination therapy to determine if this combination can effectively treat COVID-19. Treatment will last ten days. The study will last 24 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
118
Treatment with hydroxychloroquine
Treatment with azithromycin
Treatment with vitamin C
ProgenaBiome
Ventura, California, United States
The rate of recovery of mild or moderate COVID-19 in patients using Quintuple Therapy
Number of days from COVID-19 diagnosis to recovery via RT-PCR
Time frame: 12 weeks
Reduction or Progression of Symptomatic Days
Reduction and/or progression of symptomatic days, reduction of symptom severity
Time frame: 12 weeks
Assess the safety of Quintuple Therapy
Assess the symptom response to study therapy as measured by the survey in the EDC
Time frame: 12 weeks
Assess the safety of Quintuple Therapy via pulse
Pulse from baseline to 12 weeks
Time frame: 12 weeks
Assess the safety of Quintuple Therapy via oxygen saturation
Oxygen saturation from baseline to 12 weeks
Time frame: 12 weeks
Assess the safety of Quintuple Therapy via EKG
EKG response from baseline to 12 weeks
Time frame: 12 weeks
Assess Tolerability of Quintuple Therapy
Assess Adverse Events and Serious Adverse Events due to Quintuple Therapy
Time frame: 12 weeks
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Treatment with vitamin D
Treatment with Zinc