Overview

Trial Evaluating Efficacy and Safety of Anticoagulation in Patients With COVID-19 Infection, Nested in the Corimmuno-19 Cohort

Status:
Not yet recruiting
Trial end date:
2020-09-30
Target enrollment:
0
Participant gender:
All
Summary
COVID-19 is a respiratory disease caused by a novel coronavirus (SARS-CoV-2) and causes substantial morbidity and mortality. There is currently no vaccine to prevent Covid-19 or infection with SARS-CoV-2 or therapeutic agent to treat COVID-19. This protocol CORIMUNO19-COAG will evaluate the efficacy and safety of active anticoagulation using heparin: Tinzaparin (INNOHEP®) or unfractionated heparin (Calciparine®, Héparine Sodique Choay®) in COVID-19 patients hospitalized in conventional or intensive care units. It will use a phase 2 randomized open-label multicentre clinical trial, where patients will be randomly allocated to anticoagulation versus Standard of Care.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Treatments:
Calcium heparin
Dalteparin
Heparin
Heparin, Low-Molecular-Weight
Tinzaparin
Criteria
Inclusion Criteria:

1. group 1 : patients not requiring ICU at admission with mild disease to severe
pneumopathy according to The Who Criteria of severity of COVID pneumopathy, and with
symptom onset before 14 days, with need for oxygen but No non-invasive ventilation
(NIV) or High flow

2. group 2 :

- Respiratory failure AND requiring mechanical ventilation

- WHO progression scale ≥ 6

- No do-not-resuscitate order (DNR order)

Exclusion Criteria:

- Patients with contraindications to anticoagulation

1. Congenital hemorrhagic disorders

2. Hypersensitivity to tinzaparin or UHF or to any of the excipients

3. Current or history of immune-mediated heparin-induced thrombocytopenia

4. Active major haemorrhage or conditions predisposing to major haemorrhage. Major
haemorrhage is defined as fulfilling any one of these three criteria: a) occurs
in a critical area or organ (e.g. intracranial, intraspinal, intraocular,
retroperitoneal, intra-articular or pericardial, intra-uterine or intramuscular
with compartment syndrome), b) causes a fall in haemoglobin level of 20 g/L (1.24
mmol/L) or more, or c) leads to transfusion of 2 or more units of whole blood or
red blood cells.

5. Septic endocarditis

- Patients with need for anticoagulant therapy. For example: atrial fibrillation, venous
thromboembolism, mechanical valve, etc.