CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


SulodexideWiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug712 Collection of samples Wiki 1.00
drug2122 Placebo Wiki 0.05

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
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 Sulodexide in the Treatment of Early Stages of COVID-19

Problem: The COVID- 19 pandemic has not only affected our healthcare system, but the impact on the worldwide financial systems and our "normal" way of life is still to be determined. Although the percentage of patients infected with COVID-19 that need hospital care is low, Its high rate of contagiousness makes the total number of patients in need of hospital care cripple any healthcare system, limiting the space available for other patients in need of critical care, who cannot be admitted or even prefer not to attend the hospital in fear of infection. Early investigations report an Increase risk of thromboembolic complications, and a systemic inflammatory response not clearly understood. There is a possible vascular endothelial dysfunction due to chronic comorbidities (Hypertension, diabetes, obesity, chronic kidney disease, lung disease) as a risk factor for a more severe presentation. Justification: Sulodexide is a two-compound drug, each of them with different endothelial action that can be beneficial in COVID-19 patients. Glycosaminoglycans: Can help restore venous and arterial endothelial glycocalyx which can downregulate or limit the response to inflammatory molecules, by maintaining the integrity lost in certain chronic diseases (high blood pressure, diabetes). Heparin compound: It has an antithrombotic effect that could help reduce the incidence of thromboembolic complications, and also add to the anti-inflammatory response due to it anti-thrombin action (similar or a bit less to that of low molecular weight heparin) with less risk of major bleeding. It's a medication that can be used orally with minimal adverse effects and is less expensive than low molecular weight heparin. Hypothesis: We hypothesize that sulodexide instituted early in populations at significant risk and symptomatic patients affected with COVID-19 (shortness of breath, fever, weakness, diarrhoea) and risk factors of diabetes, hypertension, COPD, atherosclerosis, chronic kidney disease, will provide improvement in endothelial integrity, decrease inflammatory responses, and improved clinical outcomes with decreased hospital admission, decrease VTE and arterial complications, morbidity, and mortality. Objective: To use sulodexide in patients that have early onset of COVID-19 symptoms to mitigate the progression of the disease process that can allow them to recover at home, and limit the need of hospital care and a more severe clinical manifestation

NCT04483830 Covid19 Drug: Sulodexide Drug: Placebo

Primary Outcomes

Description: need for hospital care admission

Measure: hospital care

Time: 21 days since start of trial participation

Description: number of total days in hospital care

Measure: days of hospital care

Time: 21 days since start of trial participation

Description: total days in need of supplemental oxigen via facial mask or nasal

Measure: days of need suplemental oxigen

Time: 21 days since the start of trial participation

Description: total value in ng/dl of d-dimmer

Measure: serum level of d-dimmer

Time: change betwen basal level and at 14 day follow-up

Description: total value in mg/dl

Measure: serum level of creatinine

Time: change between basal level ans at 14 day followup

Secondary Outcomes

Description: presence of a tromboembolic event

Measure: thromboembolic event

Time: 21 days from start of trial

Description: the need for the use of endotraqueal tube mechanical ventilation

Measure: need for mechanical ventilation

Time: 21 days from the start of the trial


No related HPO nodes (Using clinical trials)