Covid 19 Research using Clinical Trials (Home Page)
Vielight RX PlusWiki
Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation
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Correlated MeSH Terms (1)
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D012818 | Signs and Symptoms, Respiratory NIH | 0.50 |
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There is one clinical trial.
Clinical Trials
The objective of this study is to obtain data on the efficacy of the Vielight RX Plus in
decreasing time to recovery of symptoms in subjects with COVID-19. The study will be
conducted among COVID-19 positive subjects at home in self-isolation via electronic data
collection (EDC). There will be no physical contact between the subjects and the Qualified
Investigator (QI) or other study staff. This study aims to demonstrate that the Vielight RX
Plus is a useful adjunct to standard of care (SOC). We hypothesize that the Vielight RX Plus
will accelerate recovery and reduce viral infection severity.
Primary Outcomes
Measure: Time to recovery Time: 30 days
Secondary Outcomes
Measure: Time to elimination of COVID-19 related symptoms Time: 30 days
Measure: Mean number of days with mild COVID-19 related symptoms Time: 30 days
Measure: Mean number of days with mild overall respiratory symptoms Time: 30 days
Measure: Time to symptom reduction Time: 30 days
Measure: Time to elimination of symptoms Time: 30 days
Measure: Average number of days with mild respiratory symptoms Time: 30 days
Measure: Oxygen saturation Time: 30 days
Measure: Hospitalization rate Time: 30 days
Measure: Mortality Time: 30 days
No related HPO nodes (Using clinical trials)