search
Back to results

Enoxaparin at Prophylactic or Therapeutic Doses in COVID-19 (EMOS-COVID)

Primary Purpose

Covid19, Thrombosis

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Enoxaparin
Sponsored by
ASST Fatebenefratelli Sacco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring COVID.19, Thrombosis, Enoxaparin, Outcome, Respiratory failure, D-dimer, Venous compression ultrasound

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • COVID-19 related pneumonia with moderate-severe respiratory failure (PaO2/FiO2<250) and/or markedly increased D-dimer level (>2000 ng/mL)
  • Signed informed consent

Exclusion Criteria:

  • age < 18 and > 80 yrs
  • history of bleeding (peptic ulcer, esophageal varices, cerebral aneurysm, cancer at high risk of bleeding, cirrhosis, hemorrhagic stroke < 1 year)
  • thrombocytopenia (<100 x109/L)
  • anemia (Hb < 8 g/dl)
  • coagulation abnormalities (PT e/o aPTT > 1.5; fibrinogen < 150 mg/dl)
  • consumption coagulopathy (ISTH criteria) [15, 16]
  • deep vein thrombosis or pulmonary embolism
  • dual antiplatelet therapy
  • ongoing anticoagulant therapy
  • allergic reaction to LMWH
  • previous heparin-induced thrombocytopenia
  • major surgery < 1 month; neurosurgery <3 months; eye surgery <3 months
  • pregnancy
  • arterial hypertension (SBPS>160 mm Hg; DBP>100 mm Hg)
  • renal failure (creatinine clearance 30 ml/min)
  • ICU admission or endotracheal intubation

Sites / Locations

  • ASST Fatebenefratelli Sacco

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Enoxaparin at prophylactic dose

Enoxaparin at therapeutic dose

Arm Description

Enoxaparin at prophylactic dose: standard 4.000 IU QD via subcutaneous injection (6000 IU if body weight>100 kg)

Enoxaparin at therapeutic dose : 70 U/Kg b.i.d. (every 12 h) In order to easily calculate the correct therapeutic dose of enoxaparin for each patient, a simplified categorization will be applied, as follows: weight < 65 Kg: 4.000 IU b.i.d. (every 12 h) weight ≥ 65 Kg: 6.000 IU b.i.d. (every 12 h) weight ≥ 100 Kg: 8.000 IU b.i.d. (every 12 h) The most appropriate dose will be evaluated in patients with creatinine clearance between 30 and 50 ml/min

Outcomes

Primary Outcome Measures

Mortality rate
Mortality registered during the time frame
Progression of respiratory failure
Progression of respiratory failure defined as duration of continuous positive pressure ventilation (CPAP)
Progression of respiratory failure
Progression of respiratory failure defined as percentage of patients admitted to ICU
Progression of respiratory failure
Progression of respiratory failure defined as percentage of patients undergoing oro-tracheal intubation
Number of major bleeding episodes
Major bleeding (ISTH criteria) and/or clinically relevant non-major bleeding

Secondary Outcome Measures

Respiratory function improvement
Amelioration of the respiratory function defined as a PaO2/FiO2 increase > 300 and / or respiratory rate (RR) < 20 breaths per min
Respiratory function improvement
Amelioration of the respiratory function defined as a PaO2/FiO2 increase > 300 and / or respiratory rate (RR) < 20 breaths per min
Number of major cardiovascular events
numbers of myocardial infarction and stroke within the time frame
Deep Vein Thrombosis
Numbers of Deep Vein Thrombosis at CUS examination within the time frame

Full Information

First Posted
November 22, 2020
Last Updated
July 22, 2023
Sponsor
ASST Fatebenefratelli Sacco
Collaborators
Massimo Arquati, Riccardo Colombo, Umberto Russo, Manuela Nebuloni, Spinello Antinori
search

1. Study Identification

Unique Protocol Identification Number
NCT04646655
Brief Title
Enoxaparin at Prophylactic or Therapeutic Doses in COVID-19
Acronym
EMOS-COVID
Official Title
Enoxaparin at Prophylactic or Therapeutic Doses With Monitoring of Outcomes in Subjects Infected With COVID-19: a Pilot Study on 300 Cases Enrolled at ASST-FBF-Sacco
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
July 27, 2020 (Actual)
Primary Completion Date
October 16, 2022 (Actual)
Study Completion Date
April 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
ASST Fatebenefratelli Sacco
Collaborators
Massimo Arquati, Riccardo Colombo, Umberto Russo, Manuela Nebuloni, Spinello Antinori

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
SINGLE CENTER PHASE III INTERVENTIONAL RANDOMIZED CONTROLLED TRIAL comparing efficacy and safety of enoxaparin at prophylactic dose (standard treatment) and enoxaparin at therapeutic dose (OFF-LABEL treatment) in 300 COVID-19 infected patients with moderate-severe respiratory failure (PaO2/FiO2<250) and/or increased D-dimer levels enrolled in different Units (Infectious disease, Internal Medicine, Emergency Medicine, Pneumology) of Azienda Socio Sanitaria Territoriale Fatebenefratelli Sacco (ASST-FBF-SACCO).
Detailed Description
Patients with COVID-19 are at high risk of developing a venous thromboembolism (VTE) and it is essential that effective thromboprophylaxis with parenteral drugs (LMWH, UFH) is considered for all patients admitted to hospital especially in case of severe pneumonia. The aim of the study is the evaluation of efficacy and safety of enoxaparin at prophylactic dose (standard treatment) as compared to enoxaparin at therapeutic dose (OFF-LABEL treatment) in 300 COVID-19 infected patients with moderate-severe respiratory failure (PaO2/FiO2<250) and/or increased D-dimer levels. After the admission to different Units (Infectious disease, Internal Medicine, Emergency Medicine, Pneumology), enoxaparin at prophylactic dose (standard of care) will be prescribed to all patients. The randomization of the single patient will be made when the the inclusion criteria (PaO2/FiO2 <250 and/or D-dimer >2000 ng/) will be satisfied. Patients with increased bleeding risk will be excluded (exclusion criteria). Patients will be divided into two arms: arm A: enoxaparin at prophylactic dose (standard 4.000 IU; 6000 UI if body weight>100 kg) arm B: enoxaparin at therapeutic dose (70 U/Kg b.i.d. every 12 h) In both arms, enoxaparin treatment will be monitored clinically and with first and second line laboratory tests Venous compression ultrasound (CUS) will be performed at admission and after 7 days in case of a first negative exam and elevated D-Dimer levels, to rule out deep vein thrombosis. Enoxaparin at prophylactic dose (4000 IU) will be maintained in all patients for 4 weeks after discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Thrombosis
Keywords
COVID.19, Thrombosis, Enoxaparin, Outcome, Respiratory failure, D-dimer, Venous compression ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
142 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enoxaparin at prophylactic dose
Arm Type
Active Comparator
Arm Description
Enoxaparin at prophylactic dose: standard 4.000 IU QD via subcutaneous injection (6000 IU if body weight>100 kg)
Arm Title
Enoxaparin at therapeutic dose
Arm Type
Experimental
Arm Description
Enoxaparin at therapeutic dose : 70 U/Kg b.i.d. (every 12 h) In order to easily calculate the correct therapeutic dose of enoxaparin for each patient, a simplified categorization will be applied, as follows: weight < 65 Kg: 4.000 IU b.i.d. (every 12 h) weight ≥ 65 Kg: 6.000 IU b.i.d. (every 12 h) weight ≥ 100 Kg: 8.000 IU b.i.d. (every 12 h) The most appropriate dose will be evaluated in patients with creatinine clearance between 30 and 50 ml/min
Intervention Type
Drug
Intervention Name(s)
Enoxaparin
Other Intervention Name(s)
Clexane
Intervention Description
subcutaneous injections
Primary Outcome Measure Information:
Title
Mortality rate
Description
Mortality registered during the time frame
Time Frame
30 days from enrollment
Title
Progression of respiratory failure
Description
Progression of respiratory failure defined as duration of continuous positive pressure ventilation (CPAP)
Time Frame
30 days from enrollment
Title
Progression of respiratory failure
Description
Progression of respiratory failure defined as percentage of patients admitted to ICU
Time Frame
30 days from enrollment
Title
Progression of respiratory failure
Description
Progression of respiratory failure defined as percentage of patients undergoing oro-tracheal intubation
Time Frame
30 days from enrollment
Title
Number of major bleeding episodes
Description
Major bleeding (ISTH criteria) and/or clinically relevant non-major bleeding
Time Frame
up to 6 months from randomization
Secondary Outcome Measure Information:
Title
Respiratory function improvement
Description
Amelioration of the respiratory function defined as a PaO2/FiO2 increase > 300 and / or respiratory rate (RR) < 20 breaths per min
Time Frame
at 72 hours
Title
Respiratory function improvement
Description
Amelioration of the respiratory function defined as a PaO2/FiO2 increase > 300 and / or respiratory rate (RR) < 20 breaths per min
Time Frame
1 week from randomization
Title
Number of major cardiovascular events
Description
numbers of myocardial infarction and stroke within the time frame
Time Frame
6 months from randomization
Title
Deep Vein Thrombosis
Description
Numbers of Deep Vein Thrombosis at CUS examination within the time frame
Time Frame
6 months from randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: COVID-19 related pneumonia with moderate-severe respiratory failure (PaO2/FiO2<250) and/or markedly increased D-dimer level (>2000 ng/mL) Signed informed consent Exclusion Criteria: age < 18 and > 80 yrs history of bleeding (peptic ulcer, esophageal varices, cerebral aneurysm, cancer at high risk of bleeding, cirrhosis, hemorrhagic stroke < 1 year) thrombocytopenia (<100 x109/L) anemia (Hb < 8 g/dl) coagulation abnormalities (PT e/o aPTT > 1.5; fibrinogen < 150 mg/dl) consumption coagulopathy (ISTH criteria) [15, 16] deep vein thrombosis or pulmonary embolism dual antiplatelet therapy ongoing anticoagulant therapy allergic reaction to LMWH previous heparin-induced thrombocytopenia major surgery < 1 month; neurosurgery <3 months; eye surgery <3 months pregnancy arterial hypertension (SBPS>160 mm Hg; DBP>100 mm Hg) renal failure (creatinine clearance 30 ml/min) ICU admission or endotracheal intubation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maddalena A Wu, M.D.
Organizational Affiliation
ASST Fatebenefratelli Sacco
Official's Role
Principal Investigator
Facility Information:
Facility Name
ASST Fatebenefratelli Sacco
City
Milan
ZIP/Postal Code
20157
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32172226
Citation
Han H, Yang L, Liu R, Liu F, Wu KL, Li J, Liu XH, Zhu CL. Prominent changes in blood coagulation of patients with SARS-CoV-2 infection. Clin Chem Lab Med. 2020 Jun 25;58(7):1116-1120. doi: 10.1515/cclm-2020-0188.
Results Reference
background
PubMed Identifier
32073213
Citation
Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020 Apr;18(4):844-847. doi: 10.1111/jth.14768. Epub 2020 Mar 13.
Results Reference
background
PubMed Identifier
32171076
Citation
Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z, Xiang J, Wang Y, Song B, Gu X, Guan L, Wei Y, Li H, Wu X, Xu J, Tu S, Zhang Y, Chen H, Cao B. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020 Mar 28;395(10229):1054-1062. doi: 10.1016/S0140-6736(20)30566-3. Epub 2020 Mar 11. Erratum In: Lancet. 2020 Mar 28;395(10229):1038. Lancet. 2020 Mar 28;395(10229):1038.
Results Reference
background
PubMed Identifier
32167524
Citation
Wu C, Chen X, Cai Y, Xia J, Zhou X, Xu S, Huang H, Zhang L, Zhou X, Du C, Zhang Y, Song J, Wang S, Chao Y, Yang Z, Xu J, Zhou X, Chen D, Xiong W, Xu L, Zhou F, Jiang J, Bai C, Zheng J, Song Y. Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease 2019 Pneumonia in Wuhan, China. JAMA Intern Med. 2020 Jul 1;180(7):934-943. doi: 10.1001/jamainternmed.2020.0994. Erratum In: JAMA Intern Med. 2020 Jul 1;180(7):1031.
Results Reference
background
PubMed Identifier
32007143
Citation
Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia J, Yu T, Zhang X, Zhang L. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507-513. doi: 10.1016/S0140-6736(20)30211-7. Epub 2020 Jan 30.
Results Reference
background
PubMed Identifier
32251717
Citation
McGonagle D, Sharif K, O'Regan A, Bridgewood C. The Role of Cytokines including Interleukin-6 in COVID-19 induced Pneumonia and Macrophage Activation Syndrome-Like Disease. Autoimmun Rev. 2020 Jun;19(6):102537. doi: 10.1016/j.autrev.2020.102537. Epub 2020 Apr 3.
Results Reference
background
PubMed Identifier
32220112
Citation
Tang N, Bai H, Chen X, Gong J, Li D, Sun Z. Anticoagulant treatment is associated with decreased mortality in severe coronavirus disease 2019 patients with coagulopathy. J Thromb Haemost. 2020 May;18(5):1094-1099. doi: 10.1111/jth.14817. Epub 2020 Apr 27.
Results Reference
background
PubMed Identifier
28963294
Citation
Iba T, Nisio MD, Levy JH, Kitamura N, Thachil J. New criteria for sepsis-induced coagulopathy (SIC) following the revised sepsis definition: a retrospective analysis of a nationwide survey. BMJ Open. 2017 Sep 27;7(9):e017046. doi: 10.1136/bmjopen-2017-017046.
Results Reference
background
PubMed Identifier
17727922
Citation
Young E. The anti-inflammatory effects of heparin and related compounds. Thromb Res. 2008;122(6):743-52. doi: 10.1016/j.thromres.2006.10.026. Epub 2007 Aug 28.
Results Reference
background
PubMed Identifier
27975101
Citation
Poterucha TJ, Libby P, Goldhaber SZ. More than an anticoagulant: Do heparins have direct anti-inflammatory effects? Thromb Haemost. 2017 Feb 28;117(3):437-444. doi: 10.1160/TH16-08-0620. Epub 2016 Dec 15.
Results Reference
background
PubMed Identifier
26064103
Citation
Mousavi S, Moradi M, Khorshidahmad T, Motamedi M. Anti-Inflammatory Effects of Heparin and Its Derivatives: A Systematic Review. Adv Pharmacol Sci. 2015;2015:507151. doi: 10.1155/2015/507151. Epub 2015 May 12.
Results Reference
background
PubMed Identifier
32239799
Citation
Thachil J. The versatile heparin in COVID-19. J Thromb Haemost. 2020 May;18(5):1020-1022. doi: 10.1111/jth.14821. Epub 2020 Apr 27. No abstract available.
Results Reference
background
PubMed Identifier
25187545
Citation
Milewska A, Zarebski M, Nowak P, Stozek K, Potempa J, Pyrc K. Human coronavirus NL63 utilizes heparan sulfate proteoglycans for attachment to target cells. J Virol. 2014 Nov;88(22):13221-30. doi: 10.1128/JVI.02078-14. Epub 2014 Sep 3.
Results Reference
background
PubMed Identifier
32302462
Citation
Barrett CD, Moore HB, Yaffe MB, Moore EE. ISTH interim guidance on recognition and management of coagulopathy in COVID-19: A comment. J Thromb Haemost. 2020 Aug;18(8):2060-2063. doi: 10.1111/jth.14860. Epub 2020 Jun 14. No abstract available.
Results Reference
background
PubMed Identifier
23379279
Citation
Wada H, Thachil J, Di Nisio M, Mathew P, Kurosawa S, Gando S, Kim HK, Nielsen JD, Dempfle CE, Levi M, Toh CH; The Scientific Standardization Committee on DIC of the International Society on Thrombosis Haemostasis. Guidance for diagnosis and treatment of DIC from harmonization of the recommendations from three guidelines. J Thromb Haemost. 2013 Feb 4. doi: 10.1111/jth.12155. Online ahead of print.
Results Reference
background
PubMed Identifier
15842354
Citation
Schulman S, Kearon C; Subcommittee on Control of Anticoagulation of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Definition of major bleeding in clinical investigations of antihemostatic medicinal products in non-surgical patients. J Thromb Haemost. 2005 Apr;3(4):692-4. doi: 10.1111/j.1538-7836.2005.01204.x.
Results Reference
background
PubMed Identifier
32437596
Citation
Ackermann M, Verleden SE, Kuehnel M, Haverich A, Welte T, Laenger F, Vanstapel A, Werlein C, Stark H, Tzankov A, Li WW, Li VW, Mentzer SJ, Jonigk D. Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19. N Engl J Med. 2020 Jul 9;383(2):120-128. doi: 10.1056/NEJMoa2015432. Epub 2020 May 21.
Results Reference
background
PubMed Identifier
32367170
Citation
Helms J, Tacquard C, Severac F, Leonard-Lorant I, Ohana M, Delabranche X, Merdji H, Clere-Jehl R, Schenck M, Fagot Gandet F, Fafi-Kremer S, Castelain V, Schneider F, Grunebaum L, Angles-Cano E, Sattler L, Mertes PM, Meziani F; CRICS TRIGGERSEP Group (Clinical Research in Intensive Care and Sepsis Trial Group for Global Evaluation and Research in Sepsis). High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study. Intensive Care Med. 2020 Jun;46(6):1089-1098. doi: 10.1007/s00134-020-06062-x. Epub 2020 May 4.
Results Reference
background

Learn more about this trial

Enoxaparin at Prophylactic or Therapeutic Doses in COVID-19

We'll reach out to this number within 24 hrs