CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 465 enrolled
Drug / intervention
Therapeutic Anticoagulationdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04362085
NCT04362085Phase 3Completed

Coagulopathy of COVID-19: A Pragmatic Randomized Controlled Trial of Therapeutic Anticoagulation Versus Standard Care as a Rapid Response to the COVID-19 Pandemic (RAPID COVID COAG)

Unity Health Toronto·interventional·Posted Apr 24, 2020·Updated Jan 30, 2025

In Brief

A Phase 3 clinical trial evaluating Therapeutic Anticoagulation for COVID-19. Completed, enrolled 465 participants across 1 site.

Detailed Summary

Coagulopathy of COVID-19 afflicts approximately 20% of patients with severe COVID-19 and is associated with need for critical care and death. COVID-19 coagulopathy is characterized by elevated D-dimer, an indicator of fibrin formation and clot lysis, and a mildly prolonged prothrombin time, suggestive of coagulation consumption. To date, it seems that COVID-19 coagulopathy manifests with thromboembolism, thus anticoagulation may be of benefit. We propose to conduct a parallel pragmatic multi-centre open-label randomized controlled trial to determine the effect of therapeutic anticoagulation compared to standard care in hospitalized patients admitted for COVID-19 with an elevated D-dimer.

Study Details

Timeline

Phase 3CompletedFinished
202120222023202420252026
First PostedApr 24, 2020
Enrollment StartMay 11, 2020
Primary CompletionMay 10, 2021
Study CompletionOct 14, 2021
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 6.2 years ago

Interventions

Therapeutic Anticoagulationdrug

The choice of low molecular weight heparin (LMWH) versus unfractionated heparin (UFH) will be at the clinician's discretion. LMWH options include: Tinzaparin, Enoxaparin or Dalteparin. UFH will be administered using a weight-based nomogram with titration according to center-specific institutional protocol.