Status:

COMPLETED

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

Lead Sponsor:

Corewell Health East

Conditions:

Covid19

Eligibility:

All Genders

18+ years

Brief Summary

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 prophyla...

Eligibility Criteria

Inclusion

  • 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

  • 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.

Key Trial Info

Start Date :

March 10 2020

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

April 15 2020

Estimated Enrollment :

704 Patients enrolled

Trial Details

Trial ID

NCT04829552

Start Date

March 10 2020

End Date

April 15 2020

Last Update

April 2 2021

Active Locations (1)

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Beaumont Health System (BHS)

Royal Oak, Michigan, United States, 48073

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