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Vielight RX PlusWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


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Name (Synonyms) Correlation

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D012818 Signs and Symptoms, Respiratory NIH 0.50

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Randomized Study Evaluating the Efficacy of the Vielight RX Plus in the Treatment of COVID-19 Respiratory Symptoms

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.

NCT04418505 COVID-19 Device: Vielight RX Plus
MeSH:Signs and Symptoms, Respiratory

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)