drugset / Trial / NCT04394377

Summary

Pragmatic randomized clinical trial of patients admitted to the hospital with confirmed COVID-19 infection and elevated D-Dimer. Randomization 1:1 - Group 1 will undergo a routine full anticoagulation (oral or parenteral when needed) strategy; and group 2 will receive usual standard of care with prophylactic anticoagulation

Timeline

Start
2020-06-21
Primary completion
2021-03-26
Completion
2021-05-30

Outcome

Missed primary endpoint

paper The primary efficacy outcome was not different between patients assigned therapeutic or prophylactic anticoagulation, with 28 899 (34·8%) wins in the therapeutic group and 34 288 (41·3%) in the prophylactic group (win ratio 0·86 [95% CI 0·59-1·22], p=0·40). PMID 34097856 ↗

paper The primary safety outcome of major or clinically relevant non-major bleeding occurred in 26 (8%) patients assigned therapeutic anticoagulation and seven (2%) assigned prophylactic anticoagulation (relative risk 3·64 [95% CI 1·61-8·27], p=0·0010). PMID 34097856 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enoxaparin sodium Other / unclassified 1 mg/kg Subcutaneous
Subject Enoxaparin sodium Other / unclassified 40 mg Subcutaneous
Subject HEPARIN CALCIUM Other / unclassified — Intravenous
Subject Rivaroxaban Other / unclassified 20 mg Oral

Indications