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Prophylactic Versus Therapeutic Dose Anticoagulation In COVID-19 Infection at the Time of Admission To Critical Care Units

William Beaumont Hospitals logo

William Beaumont Hospitals

Status

Completed

Conditions

Covid19

Study type

Observational

Funder types

Other

Identifiers

NCT04829552
2020-219

Details and patient eligibility

About

This is a multi-center, retrospective, study to determine if therapeutic dose anticoagulation (High dose group) improves inpatient mortality in severely ill patients with COVID-19 compared to prophylactic dose anticoagulation (Low dose group). The study involved 704 individuals who were admitted to Beaumont Health System (BHS) from March 10th to April 15th, 2020.

Enrollment

704 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >18 years old
  • positive reverse transcription-polymerase chain reaction (rRT-PCR) test for the qualitative detection of nucleic acid from SARS-CoV-2 in upper and lower respiratory specimens.
  • Intensive care unit (ICU) patient or Step-down unit (SDU) patient on invasive mechanical ventilation, BiPAP, 100% non-rebreather mask, or high flow oxygen or supplemental oxygen of at least 4 liters per minute nasal cannula.
  • peak d-dimer levels exceeding 1,000 mcg/mL at any time during admission.

Exclusion criteria

  • Hospital length of stay less than 5 days.
  • Hemorrhage before ICU/SDU admission.
  • Treatment with an anticoagulant other than low molecular weight heparin or unfractionated heparin.
  • Constant treatment with the same dose of anticoagulant for less than 5 days.

Trial design

704 participants in 2 patient groups

Control group: low dose group.
Description:
patients treated with subcutaneous low molecular weight heparin 40 mg once daily or unfractionated heparin 5000 IU twice or three times daily for at least 5 days.
Study group: high dose group.
Description:
Patients treated with subcutaneous low molecular weight heparin 1 mg/kg twice daily or 1.5 mg/kg daily or a continuous intravenous infusion of unfractionated heparin for at least 5 days.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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