Official Title
Enoxaparin for Thromboprophylaxis in Hospitalized COVID-19 Patients: Comparison of 40 mg o.d. Versus 40 mg b.i.d. A Randomized Clinical Trial
Brief Summary

The purpose of this study is to determine whether a higher dose of low molecular weight heparin (enoxaparin 40 mg b.i.d.) is superior than the standard prophylaxis dose (enoxaparin 40 mg o.d.) in reducing thromboembolic events in COVID-19 patients.

Detailed Description

Coronavirus disease-19 (COVID-19 ), which is caused by SARS-CoV-2 infection, are apparently
at high risk of venous thromboembolism (VTE), as a consequence of activation of the
hemostatic system which, in the most severe cases, can also be associated with the formation
of microthrombi and clinically relevant disseminated intravascular coagulation. Concerns
about the efficacy of thromboprophylaxis with standard doses of low-molecular-weight heparin
(LMWH) has been raised. Therefore, LMWH at higher doses than those recommended for
thromboprophylaxis is used in some hospitals, although no evidence exists yet of higher
efficacy of high doses compared to standard prophylactic doses. This practice might as well
increase the risk of major bleeding. The investigators designed a randomized trial comparing
standard prophylactic dose of subcutaneous enoxaparin (40 mg o.d.) with higher dose (40 mg
b.i.d) with the aim of testing whether high-dose thromboprophylaxis is more effective than
standard dose in preventing VTE in COVID-19 patients.

Completed
COVID19

Drug: Enoxaparin

Subcutaneous enoxaparin

Eligibility Criteria

Inclusion Criteria:

- All-comers patients aged >=18 years and admitted to hospital with laboratory-confirmed
SARS-CoV-2 infection

Exclusion Criteria:

- Patients admitted directly to an intensive care unit;

- Estimated creatinine clearance <15 ml/min/1.73m2;

- Patients needing anticoagulant for prior indication;

- Participants involved in other clinical trials;

- Any other significant disease or disorder which, in the opinion of the investigator,
may either put the participants at risk because of participation in the trial, or may
influence the result of the trial, or the participant's ability to participate in the
trial.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Italy
Locations

Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
Milano, Italy

Niguarda Hospital
NCT Number
Keywords
COVID19
MeSH Terms
COVID-19
Enoxaparin