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COVID-19 Antithrombotic Rivaroxaban Evaluation (CARE)

Primary Purpose

COVID-19

Status
Terminated
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Rivaroxaban 10 mg
Sponsored by
Hospital Alemão Oswaldo Cruz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring SARS-Cov-2, COVID-19, Rivaroxaban, Antithrombotic

Eligibility Criteria

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

Inclusion Criteria:

  1. Adults ≥ 18 years old;
  2. Evaluated in the emergency unit with probable or confirmed infection by COVID-19;
  3. Time between symptoms and inclusion ≤ 07 days *;
  4. Present mild or moderate signs and symptoms, with no clear indication for hospitalization;
  5. Present at least 2 risk factors for complication:

    • 65 years
    • Hypertension
    • Diabetes mellitus
    • Asthma
    • Chronic Obstructive Pulmonary Disease (COPD) or other chronic lung diseases
    • Smoking
    • Immunosuppression
    • Obesity (BMI> 30)
    • History of non-active cancer
    • Bed restriction or reduced mobility (≥50% of the wake time without walking)
    • Previous history of VTE
    • Use of oral hormonal contraceptives

Exclusion Criteria:

  1. Patients <18 years old;
  2. Hospitalization indication upon first medical care;
  3. Positive test for influenza in the first visit;
  4. Any known liver disease associated with coagulopathy; INR (International Normalized Ratio) > 1.5;
  5. Pregnant, lactating or with the possibility of becoming pregnant and without using an adequate contraceptive method;
  6. High risk of bleeding; History of bronchiectasis or pulmonary cavitation, Significant bleeding in the last 3 months, Active gastroduodenal ulcer, history of recent bleeding (within 3 months) or a high risk of bleeding;
  7. Stroke within 1 month or any history of hemorrhagic or lacunar stroke or any intracranial bleeding or any intracranial neoplasia, brain metastasis, arteriovenous malformation or brain aneurysm;
  8. Severe heart failure with left ventricular ejection fraction <30% (echocardiogram or other validated method previously documented) or symptoms of heart failure class III or IV of the New York Heart Association (NYHA);
  9. Estimated glomerular filtration rate (eGFR) <30 mL / min;
  10. Clinical indication for dual antiplatelet therapy or anticoagulation therapy (VTE, atrial fibrillation / flutter, mechanical valve prosthesis);
  11. Marked thrombocytopenia (platelets <50,000 / mm3);
  12. Non-cardiovascular disease that is associated with a poor prognosis, for example, active cancer (excluding non-melanoma skin cancer) defined as cancer without remission or requiring active chemotherapy or adjuvant therapies such as immunotherapy or radiation therapy or that increases the risk of an adverse reaction to the evaluated interventions;
  13. History of hypersensitivity or known contraindication to rivaroxaban;
  14. Systemic treatment with strong inhibitors of Cytochrome P450 3A4 (CYP3A4) and glycoprotein p (Pgp) (for example, systemic azole antimycotics, such as ketoconazole and human immunodeficiency virus [HIV] protein inhibitors, such as ritonavir) or strong inducers of CYP 3A4, that is, rifampicin, rifabutin, phenobarbital, phenytoin and carbamazepine;
  15. Current treatment being tested;
  16. Concomitant participation in another study with experimental drugs in the context of COVID;
  17. Use of chloroquine or hydroxychloroquine associated with azithromycin;
  18. Active cancer;
  19. Other contraindications to rivaroxaban;

Sites / Locations

  • Clínica Senhor do Bonfim
  • Hospital Maternidade São Vicente de Paulo
  • Hospital de Base do Distrito Federal
  • Hospital de Campanha Covid-19 Goiânia/Sesgo
  • Hospital Estadual de Urgências de Trindade/SESGO
  • Núcleo de Pesquisa Clínica do Hospital Vera Cruz
  • Hospital São Lucas
  • Santa Casa de Misericórdia de Passos
  • Hospital Universitário Regional de Maringá
  • Beneficencia Nipo Brasileira Da Amazonia
  • Hospital Adventista de Belém
  • Associação Dr. Bartholomeu Tacchini
  • Hospital São Vicente de Paulo
  • Hospital das Clínicas de Porto Alegre
  • Hospital Universitario de Santa Maria
  • Clínica Procárdio Ltda
  • H&W Cardiologia LTDA
  • Irmandade santa Casa de Araras
  • Alphacor Cardiologia Clínica e Diagnóstica LTDA
  • Maestri e Kormann Consultoria Medico-Cientifica LTDA - EPP
  • Hospital Regional do Litoral Norte - Instituto Sócrates Guanaes
  • Hospital Santos Dumont Litoral Norte
  • Hospital de Corderiopolis
  • Hospital Regional Jorge Rossman - Instituto Sócrates Guanaes
  • Hospital Carlos Fernando Malzoni
  • Hospital Moinhos de Vento
  • Hospital Regional de Registro - Instituto Sócrates Guanaes
  • Hospital Unimed Ribeirão Preto
  • Kaiser Clinica e Hospital Dia
  • Braile Hospital Dia Ltda
  • Hospital Policlin
  • Hospital Regional de São José dos Campos - Instituto Sócrates Guanaes
  • Santa Casa de Misericórdia de Votuporanga
  • International Research Center - Hospital Alemão Oswaldo Cruz
  • Hospital Leforte Liberdade
  • Incor - Instituto do Coração do Hospital das Clínicas da FMUSP

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Rivaroxaban 10 mg

Best locally standardized care

Arm Description

Participants will receive, from the 1st to the 14th day, a dose of 10 mg of rivaroxaban - OA (Oral Administration).

According to the study protocol, participating investigators are advised to follow the best available local practice in each participating site. There is no formal recommendation for any particular COVID-19 treatment, except symptomatic therapies.

Outcomes

Primary Outcome Measures

Venous thromboembolic events (VTE)
Defined as deep venous thrombosis, acute pulmonary embolism, other major venous thrombotic events.
Mechanical ventilation free-survival
Defined as survival without requirement of mechanical ventilation.
Major Adverse Cardiovascular Events (MACE)
Defined as acute myocardial infarction, stroke or acute limb ischemia
Out-of-hospital death not attributed to major injury
Death that occurred out of hospital due to any cause not related to trauma or other major injury

Secondary Outcome Measures

Time from randomization to hospitalization
Defined as time elapsed since randomization to hospital admission
Length of Hospitalization
To assess the duration of hospitalization (length of hospital stay)
Hospitalization in Intensive Care Unit
Requirement of admission to ICU for intensive care
Clinical requirement of mechanical ventilation
Requirement of oxygen supplementation through invasive or non invasive mechanical ventilation.
Clinical duration of mechanical ventilation
Total time on oxygen supplementation through invasive or non invasive mechanical ventilation
Composite vascular endpoint I
Non-fatal myocardial infarction, non-fatal ischemic stroke or cardiovascular death, VTE
Composite vascular endpoint II
Cardiovascular death, non-fatal myocardial infarction, non-fatal ischemic stroke or acute limb ischemia, VTE
Major Bleeding
Defined by International Society of Thrombosis and Hemostasis (ISTH) criteria
Mortality
Defined by all-cause deaths

Full Information

First Posted
February 8, 2021
Last Updated
January 20, 2023
Sponsor
Hospital Alemão Oswaldo Cruz
Collaborators
Bayer, Hospital Israelita Albert Einstein, Hospital do Coracao, Hospital Sirio-Libanes, Hospital Moinhos de Vento, Brazilian Research In Intensive Care Network, Brazilian Clinical Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04757857
Brief Title
COVID-19 Antithrombotic Rivaroxaban Evaluation
Acronym
CARE
Official Title
Randomized, Pragmatic, Open Controlled Multicentre Study, Evaluating the Use of Rivaroxaban in Mild or Moderate COVID-19 Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Terminated
Why Stopped
Sustained reduction in the number of new COVID-19 cases as well as lower than expected event rates
Study Start Date
September 29, 2020 (Actual)
Primary Completion Date
August 8, 2022 (Actual)
Study Completion Date
August 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Alemão Oswaldo Cruz
Collaborators
Bayer, Hospital Israelita Albert Einstein, Hospital do Coracao, Hospital Sirio-Libanes, Hospital Moinhos de Vento, Brazilian Research In Intensive Care Network, Brazilian Clinical Research Institute

4. Oversight

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

5. Study Description

Brief Summary
There are several ways in which the COVID-19 pandemic may affect the prevention and management of thrombotic and thromboembolic disease, either direct effect or the indirect effects of infection, such as through severe illness and hypoxia, may predispose patients to thrombotic events. The severe inflammatory response, critical illness, and underlying traditional risk factors may all predispose to thrombotic events. Therefore, considering the high-risk profile of cardiovascular comorbidities in patients with COVID-19, it is scientifically relevant to evaluate the use of anticoagulants as an adjunctive treatment in the context of COVID-19. Indeed, it will be tested the hypothesis that the use of moderate dose of rivaroxaban has a beneficial effect in the treatment of patients with a confirmed or probable diagnosis of COVID-19 infection, with no clear indication for hospitalization (mild and moderate cases) upon initial medical care, by reducing the need of hospitalization due to complications related to COVID-19.
Detailed Description
Initial studies suggest an inflammatory state and hypercoagulation in individuals with COVID-19. Apparently, the fact that the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein binds to Angiotensin Converting Enzyme 2 (ACE2) receptors can lead to ACE2 depletion by SARS-CoV-2 favoring the "harmful" ACE1 / angiotensin II and promoting tissue damage, including stroke. Recent observational studies indicate a higher rate of thromboembolism in patients with COVID-19, especially those in severe condition. They also report that, in patients treated with anticoagulants, complication rates were lower as compared with those not receiving anticoagulant therapies. More recently, in a post-mortem study of patients with Covid-19 compared to recently published cases of influenza, the histopathological pattern on the periphery of the lungs of patients with Covid-19 revealed a diffuse alveolar lesion with infiltration of perivascular T cells and other vascular aspects, consisting of severe endothelial damage (endothelitis) associated with the presence of intracellular viruses and broken cell membranes. In addition, pulmonary vessels showed generalized thrombosis with microangiopathy, and alveolar capillary microthrombi were much more frequent in patients with COVID-19 than with severe influenza respiratory conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
SARS-Cov-2, COVID-19, Rivaroxaban, Antithrombotic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Pragmatic, open-label, controlled randomized trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
660 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rivaroxaban 10 mg
Arm Type
Active Comparator
Arm Description
Participants will receive, from the 1st to the 14th day, a dose of 10 mg of rivaroxaban - OA (Oral Administration).
Arm Title
Best locally standardized care
Arm Type
No Intervention
Arm Description
According to the study protocol, participating investigators are advised to follow the best available local practice in each participating site. There is no formal recommendation for any particular COVID-19 treatment, except symptomatic therapies.
Intervention Type
Drug
Intervention Name(s)
Rivaroxaban 10 mg
Other Intervention Name(s)
Xarelto
Intervention Description
Rivaroxaban pharmaceutical form will be tablets of 10 mg
Primary Outcome Measure Information:
Title
Venous thromboembolic events (VTE)
Description
Defined as deep venous thrombosis, acute pulmonary embolism, other major venous thrombotic events.
Time Frame
Within 30 days from randomization
Title
Mechanical ventilation free-survival
Description
Defined as survival without requirement of mechanical ventilation.
Time Frame
Within 30 days from randomization
Title
Major Adverse Cardiovascular Events (MACE)
Description
Defined as acute myocardial infarction, stroke or acute limb ischemia
Time Frame
Within 30 days from randomization
Title
Out-of-hospital death not attributed to major injury
Description
Death that occurred out of hospital due to any cause not related to trauma or other major injury
Time Frame
Within 30 days from randomization
Secondary Outcome Measure Information:
Title
Time from randomization to hospitalization
Description
Defined as time elapsed since randomization to hospital admission
Time Frame
30 days from randomization
Title
Length of Hospitalization
Description
To assess the duration of hospitalization (length of hospital stay)
Time Frame
30 days from randomization
Title
Hospitalization in Intensive Care Unit
Description
Requirement of admission to ICU for intensive care
Time Frame
30 days from randomization
Title
Clinical requirement of mechanical ventilation
Description
Requirement of oxygen supplementation through invasive or non invasive mechanical ventilation.
Time Frame
30 days from randomization
Title
Clinical duration of mechanical ventilation
Description
Total time on oxygen supplementation through invasive or non invasive mechanical ventilation
Time Frame
30 days from randomization
Title
Composite vascular endpoint I
Description
Non-fatal myocardial infarction, non-fatal ischemic stroke or cardiovascular death, VTE
Time Frame
30 days from randomization
Title
Composite vascular endpoint II
Description
Cardiovascular death, non-fatal myocardial infarction, non-fatal ischemic stroke or acute limb ischemia, VTE
Time Frame
30 days from randomization
Title
Major Bleeding
Description
Defined by International Society of Thrombosis and Hemostasis (ISTH) criteria
Time Frame
30 days from randomization
Title
Mortality
Description
Defined by all-cause deaths
Time Frame
30 days from randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults ≥ 18 years old; Evaluated in the emergency unit with probable or confirmed infection by COVID-19; Time between symptoms and inclusion ≤ 07 days *; Present mild or moderate signs and symptoms, with no clear indication for hospitalization; Present at least 2 risk factors for complication: 65 years Hypertension Diabetes mellitus Asthma Chronic Obstructive Pulmonary Disease (COPD) or other chronic lung diseases Smoking Immunosuppression Obesity (BMI> 30) History of non-active cancer Bed restriction or reduced mobility (≥50% of the wake time without walking) Previous history of VTE Use of oral hormonal contraceptives Exclusion Criteria: Patients <18 years old; Hospitalization indication upon first medical care; Positive test for influenza in the first visit; Any known liver disease associated with coagulopathy; INR (International Normalized Ratio) > 1.5; Pregnant, lactating or with the possibility of becoming pregnant and without using an adequate contraceptive method; High risk of bleeding; History of bronchiectasis or pulmonary cavitation, Significant bleeding in the last 3 months, Active gastroduodenal ulcer, history of recent bleeding (within 3 months) or a high risk of bleeding; Stroke within 1 month or any history of hemorrhagic or lacunar stroke or any intracranial bleeding or any intracranial neoplasia, brain metastasis, arteriovenous malformation or brain aneurysm; Severe heart failure with left ventricular ejection fraction <30% (echocardiogram or other validated method previously documented) or symptoms of heart failure class III or IV of the New York Heart Association (NYHA); Estimated glomerular filtration rate (eGFR) <30 mL / min; Clinical indication for dual antiplatelet therapy or anticoagulation therapy (VTE, atrial fibrillation / flutter, mechanical valve prosthesis); Marked thrombocytopenia (platelets <50,000 / mm3); Non-cardiovascular disease that is associated with a poor prognosis, for example, active cancer (excluding non-melanoma skin cancer) defined as cancer without remission or requiring active chemotherapy or adjuvant therapies such as immunotherapy or radiation therapy or that increases the risk of an adverse reaction to the evaluated interventions; History of hypersensitivity or known contraindication to rivaroxaban; Systemic treatment with strong inhibitors of Cytochrome P450 3A4 (CYP3A4) and glycoprotein p (Pgp) (for example, systemic azole antimycotics, such as ketoconazole and human immunodeficiency virus [HIV] protein inhibitors, such as ritonavir) or strong inducers of CYP 3A4, that is, rifampicin, rifabutin, phenobarbital, phenytoin and carbamazepine; Current treatment being tested; Concomitant participation in another study with experimental drugs in the context of COVID; Use of chloroquine or hydroxychloroquine associated with azithromycin; Active cancer; Other contraindications to rivaroxaban;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Álvaro Avezum, Ph.D
Organizational Affiliation
International Research Center - Hospital Alemão Oswaldo Cruz
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clínica Senhor do Bonfim
City
Feira de Santana
State/Province
Bahia
Country
Brazil
Facility Name
Hospital Maternidade São Vicente de Paulo
City
Barbalha
State/Province
Ceará
Country
Brazil
Facility Name
Hospital de Base do Distrito Federal
City
Brasília
State/Province
Distrito Federal
Country
Brazil
Facility Name
Hospital de Campanha Covid-19 Goiânia/Sesgo
City
Goiânia
State/Province
Goias
Country
Brazil
Facility Name
Hospital Estadual de Urgências de Trindade/SESGO
City
Trindade
State/Province
Goias
Country
Brazil
Facility Name
Núcleo de Pesquisa Clínica do Hospital Vera Cruz
City
Belo Horizonte
State/Province
Minas Gerais
ZIP/Postal Code
30190-130
Country
Brazil
Facility Name
Hospital São Lucas
City
Belo Horizonte
State/Province
Minas Gerais
Country
Brazil
Facility Name
Santa Casa de Misericórdia de Passos
City
Passos
State/Province
Minas Gerais
Country
Brazil
Facility Name
Hospital Universitário Regional de Maringá
City
Maringá
State/Province
Paraná
Country
Brazil
Facility Name
Beneficencia Nipo Brasileira Da Amazonia
City
Belém
State/Province
Para
ZIP/Postal Code
66060-575
Country
Brazil
Facility Name
Hospital Adventista de Belém
City
Belém
State/Province
Para
ZIP/Postal Code
66093-904
Country
Brazil
Facility Name
Associação Dr. Bartholomeu Tacchini
City
Bento Gonçalves
State/Province
Rio Grande Do Sul
Country
Brazil
Facility Name
Hospital São Vicente de Paulo
City
Passo Fundo
State/Province
Rio Grande Do Sul
ZIP/Postal Code
99010-080
Country
Brazil
Facility Name
Hospital das Clínicas de Porto Alegre
City
Porto Alegre
State/Province
Rio Grande Do Sul
Country
Brazil
Facility Name
Hospital Universitario de Santa Maria
City
Santa Maria
State/Province
Rio Grande Do Sul
ZIP/Postal Code
97900015
Country
Brazil
Facility Name
Clínica Procárdio Ltda
City
Blumenau
State/Province
Santa Catarina
Country
Brazil
Facility Name
H&W Cardiologia LTDA
City
Joinville
State/Province
Santa Catarina
ZIP/Postal Code
89204-250
Country
Brazil
Facility Name
Irmandade santa Casa de Araras
City
Araras
State/Province
São Paulo
ZIP/Postal Code
13600-655
Country
Brazil
Facility Name
Alphacor Cardiologia Clínica e Diagnóstica LTDA
City
Barueri
State/Province
São Paulo
Country
Brazil
Facility Name
Maestri e Kormann Consultoria Medico-Cientifica LTDA - EPP
City
Blumenau
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Regional do Litoral Norte - Instituto Sócrates Guanaes
City
Caraguatatuba
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Santos Dumont Litoral Norte
City
Caraguatatuba
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital de Corderiopolis
City
Cordeiropolis
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Regional Jorge Rossman - Instituto Sócrates Guanaes
City
Itanhaém
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Carlos Fernando Malzoni
City
Matão
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Moinhos de Vento
City
Porto Alegre
State/Province
São Paulo
ZIP/Postal Code
90035-001
Country
Brazil
Facility Name
Hospital Regional de Registro - Instituto Sócrates Guanaes
City
Registro
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Unimed Ribeirão Preto
City
Ribeirão Preto
State/Province
São Paulo
Country
Brazil
Facility Name
Kaiser Clinica e Hospital Dia
City
São José do Rio Preto
State/Province
São Paulo
ZIP/Postal Code
15015-110
Country
Brazil
Facility Name
Braile Hospital Dia Ltda
City
São José Do Rio Preto
State/Province
São Paulo
Country
Brazil
Facility Name
Hospital Policlin
City
São José Dos Campos
State/Province
São Paulo
ZIP/Postal Code
12 243 000
Country
Brazil
Facility Name
Hospital Regional de São José dos Campos - Instituto Sócrates Guanaes
City
São José Dos Campos
State/Province
São Paulo
Country
Brazil
Facility Name
Santa Casa de Misericórdia de Votuporanga
City
Votuporanga
State/Province
São Paulo
Country
Brazil
Facility Name
International Research Center - Hospital Alemão Oswaldo Cruz
City
São Paulo
ZIP/Postal Code
01323-903
Country
Brazil
Facility Name
Hospital Leforte Liberdade
City
São Paulo
ZIP/Postal Code
01506-000
Country
Brazil
Facility Name
Incor - Instituto do Coração do Hospital das Clínicas da FMUSP
City
São Paulo
ZIP/Postal Code
05403-010
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No

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COVID-19 Antithrombotic Rivaroxaban Evaluation

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