CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


ZincWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (19)


Name (Synonyms) Correlation
drug2662 Vitamin C Wiki 0.49
drug1278 Ivermectin Injectable Solution Wiki 0.41
drug1018 Guided online support program Wiki 0.41
drug1015 Group1 Wiki 0.41
drug1975 Quercetin Wiki 0.41
drug1275 Ivermectin 3Mg Tab Wiki 0.41
drug2771 bromelain Wiki 0.41
drug2010 RT PCR SARS-CoV-2 Wiki 0.41
drug1088 Hydroxychloroquine (placebo) Wiki 0.41
drug3044 vitamin d Wiki 0.41
drug2716 Zinc (Placebo) Wiki 0.41
drug2676 WHO recommendations (waiting condition) Wiki 0.41
drug2663 Vitamin D Wiki 0.31
drug1595 Nigella Sativa / Black Cumin Wiki 0.29
drug1115 Hydroxychloroquine Sulfate Tablets Wiki 0.29
drug1883 Povidone-Iodine Wiki 0.20
drug1086 Hydroxychloroquine Wiki 0.12
drug262 Azithromycin Wiki 0.07
drug1822 Placebo Wiki 0.02

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D011248 Pregnancy Complications NIH 0.17
D003141 Communicable Diseases NIH 0.11
D045169 Severe Acute Respiratory Syndrome NIH 0.10
D007239 Infection NIH 0.09
D018352 Coronavirus Infections NIH 0.08

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 6 clinical trials

Clinical Trials


1 A Randomized, Double-Blind, Placebo-Controlled Phase IIa Study of Quintuple Therapy to Treat COVID-19 Infection

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).

NCT04334512 COVID-19 Corona Virus Infection Coronavirus-19 Sars-CoV2 Drug: Hydroxychloroquine Drug: Azithromycin Dietary Supplement: Vitamin C Dietary Supplement: Vitamin D Dietary Supplement: Zinc
MeSH:Infection Communicable Diseases Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: Number of days from COVID-19 diagnosis to recovery via RT-PCR

Measure: The rate of recovery of mild or moderate COVID-19 in patients using Quintuple Therapy

Time: 12 weeks

Description: Reduction and/or progression of symptomatic days, reduction of symptom severity

Measure: Reduction or Progression of Symptomatic Days

Time: 12 weeks

Description: Assess the symptom response to study therapy as measured by the survey in the EDC

Measure: Assess the safety of Quintuple Therapy

Time: 12 weeks

Description: Pulse from baseline to 12 weeks

Measure: Assess the safety of Quintuple Therapy via pulse

Time: 12 weeks

Description: Oxygen saturation from baseline to 12 weeks

Measure: Assess the safety of Quintuple Therapy via oxygen saturation

Time: 12 weeks

Description: EKG response from baseline to 12 weeks

Measure: Assess the safety of Quintuple Therapy via EKG

Time: 12 weeks

Description: Assess Adverse Events and Serious Adverse Events due to Quintuple Therapy

Measure: Assess Tolerability of Quintuple Therapy

Time: 12 weeks

2 A Randomized, Double-Blind, Placebo-Controlled Phase IIa Study of Hydroxychloroquine, Vitamin C, Vitamin D, and Zinc for the Prevention of COVID-19 Infection

This is a Phase II interventional study testing whether treatment with hydroxychloroquine, Vitamin C, Vitamin D, and Zinc can prevent symptoms of COVID-19

NCT04335084 COVID-19 Coronavirus Infection Sars-CoV2 Corona Virus Infection COVID Coronavirus Coronavirus-19 Coronavirus 19 Drug: Hydroxychloroquine Dietary Supplement: Vitamin C Dietary Supplement: Vitamin D Dietary Supplement: Zinc
MeSH:Infection Communicable Diseases Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: Any symptoms of COVID-19 will be recorded in a daily diary. Symptoms (including fever measured in degrees Fahrenheit, dry cough, productive cough, difficulty speaking, wheezing, dry mouth, headache, chest tightness, difficulty with exertion, shortness of breath, sore throat, malaise, and diarrhea) will be rated as not present, mild, moderate, or severe.

Measure: Prevention of COVID-19 symptoms as recorded in a daily diary

Time: 24 weeks

Description: To assess the presence or absence of side effects (graded 1-5), and whether they are tolerable (grade 1-2). AE and SAE will be recorded.

Measure: Safety as determined by presence or absence of Adverse Events and Serious Adverse Events

Time: 24 weeks

3 A Study of Hydroxychloroquine and Zinc in the Prevention of COVID-19 Infection in Military Healthcare Workers (COVID-Milit)

A multicenter randomized clinical trial aiming to assess the efficacy of hydroxychloroquine associated to Zinc compared to hydroxychloroquine, in the prevention of Military Health Professionals Exposed to SARS CoV2 in Tunisia

NCT04377646 Sars-CoV2 COVID19 Drug: Hydroxychloroquine Drug: Hydroxychloroquine (placebo) Drug: Zinc Drug: Zinc (Placebo)
MeSH:Infection

Primary Outcomes

Description: Frequency of confirmed SARS CoV2 infection

Measure: SARS CoV2 infection

Time: At 2 months of follow-up

Secondary Outcomes

Description: Any COVID-19 related symptoms (cough, fever, headache, vomiting, nausea, dyspnea, diarrhea, smell disorder,conjunctivitis, dizziness)

Measure: COVID-19 symptoms description

Time: At 2 months of follow-up

Description: Any adverse event or serious adverse event

Measure: Adverse Events

Time: each month up to 2 months

4 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

5 The Study of Quadruple Therapy Zinc, Quercetin, Bromelain and Vitamin C on the Clinical Outcomes of Patients Infected With COVID-19

There are currently no antiviral drugs with proven efficacy nor are there vaccines for its prevention. Unfortunately, the scientific community has little knowledge of the molecular details of SARS-CoV-2 infection. The drugs we are chosen are used as clinical trials for antiviral and there is no proven guide for specificity and effectiveness against the virus so the results are different Now the clinical trials and research authorities are work speedily to target the most proven treatment for the virus so anything is infantile until now. the covid-19 with time be more explained by scientists it is steroid response disease and cause thromosis and cytokine storm , the aim of the study to inhibit viral replication and decrease the severity of the disease as antiviral and anticytokine storm , antithrombosis Zinc is a mineral element needed to regulate adaptive immune cells' functions. Higher level of intracellular zinc showed to increase intracellular pH; which affect on RNA-dependent RNA polymerase and decrease replication mechanism of RNA viruses. Therefore, drugs that described as zinc ionophores could be used with zinc supplement to act as antiviral against many RNA viruses including SARS-CoV-2 Quercetin is natural compound act as zinc ionophore to cause zinc influx intracellular. Quercetin is a safe natural anti-oxidant and anti-inflammatory polyphenolic compound that found in various natural sources include onion, red grapes, honey and citrus fruits. It was shown that quercetin has the ability to chelate zinc ions and act as zinc ionophore. Therefore, quercetin could have antiviral activity against many RNA viruses . Quercetin, a flavonoid found in fruits and vegetables, has unique biological properties that may improve mental/physical performance and reduce infection risk ; These properties form the basis for potential benefits to overall health and disease resistance, including anti-carcinogenic, anti-inflammatory, antiviral, antioxidant, and psychostimulant activities, as well as the ability to inhibit lipid peroxidation, platelet aggregation and capillary permeability, and to stimulate mitochondrial biogenesis .There are various studies that report the immunomodulatory effect of bromelain . Bromelain activates natural killer cells and augments the production of granulocyte-macrophage-colony stimulating factor, IL-2, IL-6 and decreases the activation of Thelper cells. Thus, bromelain decreases the majority of inflammatory mediators and has demonstrated a significant role as an anti-inflammatory agent in various conditions Vitamin C is known as an essential anti-oxidant.,and enzymatic co-factor for physiological reactions such as hormone production, collagen synthesis and immune potentiation . Naturally, an insufficiency of vitamin C leads to severe injuries to multiple organs, especially to the heart and brain, since they are both highly aerobic organs that produce more oxygen radicals. In fact, studies of in vivo effect on vitamin C are difficult since most animals, except human and some primate, are capable of synthesizing vitamin C endogenously

NCT04468139 Covid-19 Drug: Quercetin Dietary Supplement: bromelain Drug: Zinc Drug: Vitamin C

Primary Outcomes

Description: speed the days of recovery and discharge from hospital

Measure: days of stay at hospital after treatment and discharge

Time: 28 days

Description: the level of serum zinc is very important especially at chronic diseases

Measure: serum zinc before and after treatment

Time: 5-10 days

Secondary Outcomes

Description: according to questionnaire including BMI, smoking , underlying diseases like hypertension, diabetes , asthmatic , ..etc

Measure: questionnaire including parameters like BMI,,smoking , underling diseases, immunological treatment ,

Time: 28 days

Description: day of negative conversion for nasopharyngeal swab for rt-PCR FOR covid-19

Measure: day of negative conversion for nasopharyngeal swab for rt-PCR FOR covid-19

Time: 28 days

6 Sub-cutaneous Ivermectin in Combination With and Without Oral Zinc and Nigella Sativa: a Placebo Randomized Control Trial on Mild to Moderate COVID-19 Patients

To measure the effect of Ivermectin (sub-cutaneous) with or without zinc and Nigella sativa in treating the COVID-19 patients to clear viral load of SARS-CoV-2 along with reduction in severity of symptoms and length of hospitalization of patients with COVID-19.

NCT04472585 Coronavirus Infection COVID Sars-CoV2 Drug: Nigella Sativa / Black Cumin Drug: Ivermectin Injectable Solution Other: Placebo Drug: Zinc
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: time needed to turn positive COVID-19 PCR to negative

Measure: qRT-PCR

Time: 14 days

Secondary Outcomes

Description: time needed to make patients clinically better

Measure: Severity of symptoms

Time: 14 days


No related HPO nodes (Using clinical trials)