Enoxaparin at Prophylactic or Therapeutic Doses in COVID-19 (EMOS-COVID)
Covid19, Thrombosis
About this trial
This is an interventional treatment trial for Covid19 focused on measuring COVID.19, Thrombosis, Enoxaparin, Outcome, Respiratory failure, D-dimer, Venous compression ultrasound
Eligibility Criteria
Inclusion Criteria:
- COVID-19 related pneumonia with moderate-severe respiratory failure (PaO2/FiO2<250) and/or markedly increased D-dimer level (>2000 ng/mL)
- Signed informed consent
Exclusion Criteria:
- age < 18 and > 80 yrs
- history of bleeding (peptic ulcer, esophageal varices, cerebral aneurysm, cancer at high risk of bleeding, cirrhosis, hemorrhagic stroke < 1 year)
- thrombocytopenia (<100 x109/L)
- anemia (Hb < 8 g/dl)
- coagulation abnormalities (PT e/o aPTT > 1.5; fibrinogen < 150 mg/dl)
- consumption coagulopathy (ISTH criteria) [15, 16]
- deep vein thrombosis or pulmonary embolism
- dual antiplatelet therapy
- ongoing anticoagulant therapy
- allergic reaction to LMWH
- previous heparin-induced thrombocytopenia
- major surgery < 1 month; neurosurgery <3 months; eye surgery <3 months
- pregnancy
- arterial hypertension (SBPS>160 mm Hg; DBP>100 mm Hg)
- renal failure (creatinine clearance 30 ml/min)
- ICU admission or endotracheal intubation
Sites / Locations
- ASST Fatebenefratelli Sacco
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Enoxaparin at prophylactic dose
Enoxaparin at therapeutic dose
Enoxaparin at prophylactic dose: standard 4.000 IU QD via subcutaneous injection (6000 IU if body weight>100 kg)
Enoxaparin at therapeutic dose : 70 U/Kg b.i.d. (every 12 h) In order to easily calculate the correct therapeutic dose of enoxaparin for each patient, a simplified categorization will be applied, as follows: weight < 65 Kg: 4.000 IU b.i.d. (every 12 h) weight ≥ 65 Kg: 6.000 IU b.i.d. (every 12 h) weight ≥ 100 Kg: 8.000 IU b.i.d. (every 12 h) The most appropriate dose will be evaluated in patients with creatinine clearance between 30 and 50 ml/min