CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Ivermectin 3Mg TabWiki

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


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug2010 RT PCR SARS-CoV-2 Wiki 1.00
drug1115 Hydroxychloroquine Sulfate Tablets Wiki 0.71
drug1883 Povidone-Iodine Wiki 0.50
drug2715 Zinc Wiki 0.41
drug2662 Vitamin C Wiki 0.30

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D011248 Pregnancy Complications NIH 0.41
D003141 Communicable Diseases NIH 0.09
D007239 Infection NIH 0.06
D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Randomized Open-label Prophylaxis Trial Among Migrant Workers at High-risk of Covid-19 (DORM Trial)

In December 2019, a novel coronavirus, now called COVID-19, emerged as a global health threat from Wuhan, China. Within weeks, the contagious virus spread within and between communities, causing a lower respiratory tract infection dominated by symptoms of fever, cough and sore throat. The incubation period was estimated at between 5 to 7 days, but could last as long as 14 days. Although COVID-19 causes a mostly mild and self-limiting disease, respiratory involvement has been reported in about 5% of the population, requiring supplemental oxygen and even ventilatory support to relieve hypoxia. Alveolar damage, fibrosis and consolidation have been reported in radiologic and post-mortem studies. Existing data suggest a mortality rate of COVID-19 is approximately 1-2%, higher among individuals with pre-existing comorbidities and in healthcare systems with suboptimal access to ventilatory support. Given its high transmissibility, COVID-19 has quickly spread across the globe within a short interval. By 27 April 2020, over 3 million people around the world have been diagnosed with COVID-19, and more 200,000 have succumbed to the disease. As a proportion of patients manifest mild or no symptoms, these numbers are likely an underestimate of the actual number of patients with COVID-19. More disconcertingly, patients are known to shed viruses despite mild or no symptoms, making it essential that a collective approach against COVID-19 incorporate active pharmacological treatment to prevent or mitigate virus pathogenesis prior to its potential evolution to cause respiratory distress. To date, clinical trials have focused on the treatment of hospitalised patients diagnosed with COVID-19; only few have examined the clinical benefits of pharmacological agents despite few compelling in vitro data. The relatively high transmission of COVID-19 in a closed dormitory environment of migrant workers in Singapore presents a real-life scenario where a prophylaxis treatment could reduce the impact of the disease. In Singapore, there are well grounded concerns an excess in cases could pose the possibility of strain in healthcare system and mentally drain her workers. The availability of an effective prophylaxis treatment is highly desirable to potentially reduce this burden. Data from the current study could also have implications on how future outbreaks in high-density areas should be managed, especially when residents are subjected to quarantine and isolation.

NCT04446104 Covid-19 Drug: Hydroxychloroquine Sulfate Tablets Drug: Ivermectin 3Mg Tab Drug: Zinc Drug: Povidone-Iodine Dietary Supplement: Vitamin C

Primary Outcomes

Description: Acute respiratory illness is defined by acute onset with any key respiratory symptoms including cough, shortness of breath, sore throat, runny nose and change in smell.

Measure: Incidence of acute respiratory illness in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Secondary Outcomes

Measure: Incidence of febrile respiratory illness in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Rate of hospitalization for COVID-19 and non-COVID-19 related indications in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Rate of oxygen supplementation and mechanical ventilation in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Duration of oxygen supplementation and mechanical ventilation in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Length of hospital stay in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Rate of laboratory-confirmed COVID-19 in treatment arms (hydroxycholorquine, ivermectin, zinc and povidone iodine)

Time: At the end of study dosing, which is day 42

Measure: Incidence of adverse events and serious adverse events in control arm (Vitamin C)

Time: At the end of study dosing, which is day 42

Measure: Incidence of drug discontinuation due to adverse events in control arm (Vitamin C)

Time: At the end of study dosing, which is day 42


No related HPO nodes (Using clinical trials)