CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Routine care for COVID-19 patientsWiki

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


Correlated Drug Terms (6)


Name (Synonyms) Correlation
drug1062 High-Titer Anti-SARS-CoV-2 (COVID 19) Convalescent Plasma Wiki 0.71
drug2956 plasma therapy using convalescent plasma with antibody against SARS-CoV-2 Wiki 0.71
drug1363 Lopinavir and Ritonavir Tablets Wiki 0.71
drug208 Arbidol Wiki 0.50
drug923 Favipiravir Wiki 0.17
drug1086 Hydroxychloroquine Wiki 0.07

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D007239 Infection NIH 0.08
D045169 Severe Acute Respiratory Syndrome NIH 0.07
D003141 Communicable Diseases NIH 0.06
D018352 Coronavirus Infections NIH 0.06
D011014 Pneumonia NIH 0.04

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.04

There are 2 clinical trials

Clinical Trials


1 Use of Convalescent Plasma Therapy for COVID-19 Patients With Hypoxia: a Prospective Randomized Trial

Plasma therapy using convalescent plasma has been shown to be effective in severe acute respiratory syndrome, Ebola virus infection and in H1N1 influenza. More recently there has been a report of the use of convalescent plasma in the treatment of 5 ventilated COVID-19 patients with the suggestion of expedited recovery as the patients improved 1 week after the transfusion. However, this was not a clinical trial and the patients were on other antiviral medication.; therefore, there is a need to undertake such a trial to see if deploying plasma with SARS-CoV-2 neutralizing antibody has utility in managing patients infected with COVID-19 in respiratory distress. The objective of this pilot study is to compare plasma therapy using convalescent plasma with antibody against SARS-CoV-2 to usual supportive therapy in COVID-19 patients with pneumonia and hypoxia, and to determine if the clinical course is improved. The difference between groups will allow an effect size to be determined for a definitive clinical trial.

NCT04356534 SARS-CoV 2 COVID-19 Other: plasma therapy using convalescent plasma with antibody against SARS-CoV-2 Other: Routine care for COVID-19 patients

Primary Outcomes

Description: Could the plasma therapy avoid or delay the need for invasive ventilation

Measure: Requirement for invasive ventilation

Time: through study completion up to 28 days

Secondary Outcomes

Description: Through the use of CT values

Measure: Change in viral clearance

Time: through study completion up to 28 days

Description: Chest Xray

Measure: Radiological change

Time: through study completion up to 28 days

Description: As a measure of a change in inflammation

Measure: Change in white cell count

Time: through study completion up to 28 days

Description: A change in C reactive protein as a measure of a change in inflammation

Measure: C reactive protein measurement

Time: through study completion up to 28 days

Description: A change in lactate dehydrogenase as a measure of an improvement in the severity of the disease process

Measure: lactate dehydrogenase measurement

Time: through study completion up to 28 days

Description: A change in procalcitonin as a measure of an improvement in the severity of the disease process

Measure: Procalcitonin measurement

Time: through study completion up to 28 days

Description: A change in D Dimer as a measure of an improvement in the severity of the disease process

Measure: D Dimer measurement

Time: through study completion up to 28 days

Description: A change in Ferritin as a measure of an improvement in the severity of the disease process

Measure: Ferritin measurement

Time: through study completion up to 28 days

Description: A change in troponin T as a measure of an improvement in the severity of the disease process

Measure: Troponin T measurement

Time: through study completion up to 28 days

Description: A change in brain naturetic peptide as a measure of an improvement in the severity of the disease process

Measure: Brain naturetic peptide measurement

Time: through study completion up to 28 days

Description: Mortality rate due to COVID-19

Measure: Mortality rate

Time: Up to 28 days of the study

2 Treatment of Covid-19 With Favipiravir Versus Hydroxychloroquine: a Randomized Comparator Trial

Hydroxychloroquine is widely used to treat autoimmune diseases. Clinical investigation has found that a high concentration of cytokines were detected in the plasma of critically ill patients infected with SARS-CoV-2, therefore, hydroxychloroquine as anti-inflammatory agents may reduce this response in accord with their use in autoimmune disease where the cytokine response can be reduced. Favipiravir is an antiviral drug developed in Japan that the data sheet notes that it is a pyrazinecarboxamide derivative with activity against influenza viruses, west nile virus, yellow fever virus, foot and mouth disease virus as well as against flaviviruses, arenaviruses, bunyaviruses and alphaviruses. In February the drug was used for COVID-19 disease in China and was declared effective in treatment, and a report published (in press) comparing Favipiravir with Lopinavir /ritonavir suggested that Favipiravir was superior for prevention of disease progression and viral clearance. The objective of this pilot study is to compare three arms: hydroxychloroquine; favipiravir; standard care (no specific SARS-CoV-2 treatment) only, in symptomatic patients infected by SARS-CoV-2 in an open label randomized clinical trial. The difference between groups will allow an effect size to be determined for a definitive clinical trial.

NCT04387760 SARS-CoV 2 COVID-19 Drug: Hydroxychloroquine Drug: Favipiravir Other: Routine care for COVID-19 patients

Primary Outcomes

Description: Single negative SARS-CoV2 PCR NP Swab

Measure: Primary outcome measure will be time to viral clearance

Time: Until discharge or for a maximum of 14 days or readmission

Secondary Outcomes

Description: Implementation of escalation of Respiratory Support

Measure: Requirement of Escalation of Respiratory Support

Time: Until discharge or for a maximum of 14 days or readmission

Description: Monitor and document all adverse effects during therapy

Measure: Adverse effects(cardiac, renal, hepatic, hypoglycaemia (defined as RBS <3.9 mmol/L))

Time: Until discharge or for a maximum of 14 days or readmission

Description: Deterioration of clinical condition requiring ICU admission

Measure: Requirement of ICU Admission

Time: Until discharge or for a maximum of 14 days or readmission

Description: Mortality rate due to COVID-19

Measure: Mortality rate

Time: Mortality will be collected up to 30 day

Description: Determination of the change in lactate levels before and after treatment as a measure of disease activity

Measure: Serum lactate measurement

Time: Until discharge or for a maximum of 14 days or readmission

Description: Determination of the change in ferritin levels before and after treatments as a measure of disease activity

Measure: Serum Ferritin measurement

Time: Until discharge or for a maximum of 14 days or readmission

Description: Determination of the change in D Dimer levels before and after treatments as a measure of disease activity

Measure: Serum D Dimer measurement

Time: Until discharge or for a maximum of 14 days or readmission

Description: Determination of the change in Ratio of Lymphocyte to Neutrophil, before and after treatments as a measure of disease activity

Measure: Ratio of Lymphocyte to Neutrophil, measurement

Time: Until discharge or for a maximum of 14 days or readmission

Description: Patients will be followed during their hospital stay until discharge

Measure: Discharge and Length of Hospital Stay

Time: Until discharge or for a maximum of 14 days or readmission

Description: Capturing readmission data

Measure: Readmission Rate

Time: Until 30 days from the start of the trial

Description: SOFA score can identify the critical point at which patients exhibit the highest degree of organ dysfunction

Measure: Daily Sequential Organ Failure Assessment (SOFA) score

Time: Until discharge or for a maximum of 14 days or readmission

Description: NEWS is a tool which improves the detection and response to clinical deterioration in adult patients and is a key element of patient safety and improving patient outcomes

Measure: Daily National Early Warning Score (NEWS) 2 score

Time: Until discharge or for a maximum of 14 days or readmission

Description: its defined as patient discharge or a reduction of 2 points on a 6-point disease severity clinical scale

Measure: Clinical improvement

Time: Until discharge or for a maximum of 14 days or readmission

Description: Determination of the change in QT prolongation, before and after treatments as a measure of disease activity

Measure: QT prolongation

Time: Until discharge or for a maximum of 14 days or readmission

Description: Determination of the change in Cardiac arrythmia (fatal and non fatal), before and after treatments as a measure of disease activity

Measure: Cardiac arrythmia (fatal and non fatal)

Time: Until discharge or for a maximum of 14 days or readmission


No related HPO nodes (Using clinical trials)