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Nebulized Heparin in Severe Acute Respiratory Syndrome COVID-19 (NEBUHEPA)

Primary Purpose

Covid19, Pneumonia

Status
Unknown status
Phase
Phase 4
Locations
Argentina
Study Type
Interventional
Intervention
Heparin sodium
Enoxaparin
Sponsored by
Clinica San Camilo, Argentina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring nebulized heparin pneumonia COVID 19

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Persons over 18 years of age of any sex admitted with a diagnosis of a suspected case of COVID-19, in accordance with the definition of the Ministry of Health of the Nation (MSal) as of May 20, 2020, who present at the time of admission or in its evolution pulmonary infiltrates compatible with imaging studies (chest X-ray or chest CT) and at least one of the following biochemical parameters of systemic inflammation:

    • D DIMER over 1.0 ug/dl
    • Ferritin over 500 ng/ml
    • Fibrinogen over 500 mg/dl

Exclusion Criteria:

  • Under 18 years old
  • Pregnant women
  • Known allergy to Heparin
  • Participant in another clinical trial that is not approved for joint enrollment.
  • APTT> 120 seconds, not due to anticoagulant therapy.
  • Platelet count <20 x 109 per L
  • Lung bleeding.
  • Uncontrolled bleeding
  • Advanced neurological impairment
  • Advanced oncological disease

Sites / Locations

  • Clinica San CamiloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

NEBULIZED HEPARIN

Enoxaparine

Arm Description

Nebulized Heparin (UNF)5000 IU in Saline Solution1 ml every 8 hours plus Enoxaparine 40mg /d or 60mg/d, adjusted by BMI and calculated creatinine clearance . Device to nebulize without producing aerosolization: To nebulized heparin we have a modified a fullface snorkel mask, in which instead of the discharge valve a connector for the Venturi has been placed, and in the air outlet / inlet of the snorkel it has been adapted a connector made with 3D printing for the insertion of a disposable antiviral filter (filters commonly used in Mechanical Respiratory Assistance devices). The mask is made of materials that allow its sterilization with the STERRAT Hydrogen Peroxide plasma system, available at the institution.

Enoxaparin 40mg/d or 60mg/d adjusted by BMI and calculated creatinine clearance

Outcomes

Primary Outcome Measures

Percentage of patients requirement mechanical ventilation
Blood Gas criteria :PaO2 / FiO2 <200 (or the inability to maintain an SpO2 of at least 92% with a reservoir mask). Acute ventilatory failure (pH less than 7.35 with PaCO2 greater than 45 mmHg)

Secondary Outcome Measures

Percentage of patients with PaO2 to Fi02 ratio > 300
Mean every 48 hours PaO2 to FiO2 ratio
Lengths of hospital-stay
To compare the lengths of hospital-stay
Mortality rate
All cause mortality

Full Information

First Posted
August 17, 2020
Last Updated
August 27, 2020
Sponsor
Clinica San Camilo, Argentina
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1. Study Identification

Unique Protocol Identification Number
NCT04530578
Brief Title
Nebulized Heparin in Severe Acute Respiratory Syndrome COVID-19
Acronym
NEBUHEPA
Official Title
Efficacy and Safety Study to Evaluate the Use of Nebulized Heparin in Patients With Severe Acute Respiratory Syndrome Covid-19 (SARS-CoV-2)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
October 30, 2020 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clinica San Camilo, Argentina

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate the safety and efficacy of the use of inhalational heparin in patients with pulmonary compromise / pneumonia / SARS associated with COVID-19, laboratory with marked inflammation parameters, and prothrombotic state secondary to it (Fibrinogen, Ferritin and / or elevated D-Dimer) , from admission to hospitalization. The combination of inhalation heparin combined with prophylactic doses of LMWH could reduce the progression to severe forms of the disease, and consequently the need for intensive care units and mechanical ventilation.
Detailed Description
The emergency of COVID-19 requires the urgent development of strategies to avoid the impact of the disease on our population, the saturation of the health system and the mortality of the disease. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in Wuhan, Hubei province, China and has subsequently spread to the world population. Factors associated with the development of SARS and its mortality include advanced age, lymphopenia, organ dysfunction, and bleeding disorders. Different manifestations have been described (deep vein thrombosis, pulmonary thromboembolism, digital ischemia and cerebral infarcts), and different mechanisms, such as the presence of antiphospholipid antibodies in COVID-19. There is evidence of the presence of a hypercoagulable state in the majority of deaths from SARS associated with COVID -19. Increased plasma D-dimer concentrations is a common finding and also appears to be an independent predictor of mortality. These patients and those who meet criteria for sepsis-induced coagulopathy (SIC) would benefit from anticoagulant therapy primarily with low molecular weight heparin (LMWH). Antithrombotic therapies have been used in clinical practice for almost a century. In clinical practice, unfractionated heparin (UFH) and heparin derivatives remain the predominant antithrombotic therapies administered parenterally. Heparin binds to antithrombin III (AT-III), a plasma glycoprotein, and to a small extent also to the heparin II cofactor. The result of this binding produces a conformational change and a strong increase in the inhibitory effect of thrombin, which becomes approximately 1000 times more potent than before. Other targets of heparin on coagulation are the inhibition or reduced activation of factors V, VIII and IX and the inhibition of thrombocyte function, due to a nonspecific binding of platelet factor IV. However, heparin is a drug not only with anticoagulant properties, it has many other properties (interaction with growth factors, regulation of cell proliferation and angiogenesis, modulation of proteases and antiproteases), making it an interesting subject of research in the field of inflammation, allergy and immunology, interstitial lung fibrosis and oncology. Inhalation of heparin produces local anti-inflammatory and antifibrotic effects . In addition, possible effects have been described to prevent viral infection, including coronaviridae . It was describes the capacity of SARS-CoV-2 S1 RBD to bind heparin. Such binding capacity is an important prerequisite for research related to the development of SARS-CoV-2 unfractionated heparin therapeutic inhalation Experimental studies of inhaled UFH in healthy subjects showed that doses of less than 32,000 IU of UFH through the lower respiratory tract were safe. In a prospective cohort study in young adults, Harenberg determined that the inhaled dose of LMWH had to be 10 times greater than that administered subcutaneously to achieve similar levels of anti-factor Xa assay. Considering the role of coagulopathy and inflammation in the induction of ventilator-induced lung injury, nebulized heparin improved lung function in ventilated patients, equivalent to the use of corticosteroids. It has also been compared with other interventions to stimulate the fibrinolysis or block coagulation to suppress the inflammatory response and reduce lung injury in adult acute respiratory distress syndrome .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Pneumonia
Keywords
nebulized heparin pneumonia COVID 19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Controled, prospective, randomized, comparative against standard treatment.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
NEBULIZED HEPARIN
Arm Type
Experimental
Arm Description
Nebulized Heparin (UNF)5000 IU in Saline Solution1 ml every 8 hours plus Enoxaparine 40mg /d or 60mg/d, adjusted by BMI and calculated creatinine clearance . Device to nebulize without producing aerosolization: To nebulized heparin we have a modified a fullface snorkel mask, in which instead of the discharge valve a connector for the Venturi has been placed, and in the air outlet / inlet of the snorkel it has been adapted a connector made with 3D printing for the insertion of a disposable antiviral filter (filters commonly used in Mechanical Respiratory Assistance devices). The mask is made of materials that allow its sterilization with the STERRAT Hydrogen Peroxide plasma system, available at the institution.
Arm Title
Enoxaparine
Arm Type
Active Comparator
Arm Description
Enoxaparin 40mg/d or 60mg/d adjusted by BMI and calculated creatinine clearance
Intervention Type
Drug
Intervention Name(s)
Heparin sodium
Other Intervention Name(s)
UNFRACTION HEPARIN
Intervention Description
Nebulized Heparin every 8 hours plus Subcutaneous Enoxaparin every 24hours
Intervention Type
Drug
Intervention Name(s)
Enoxaparin
Other Intervention Name(s)
Low Molecular Weight Heparin
Intervention Description
Subcutaneous Enoxaparine every 24 hours
Primary Outcome Measure Information:
Title
Percentage of patients requirement mechanical ventilation
Description
Blood Gas criteria :PaO2 / FiO2 <200 (or the inability to maintain an SpO2 of at least 92% with a reservoir mask). Acute ventilatory failure (pH less than 7.35 with PaCO2 greater than 45 mmHg)
Time Frame
15 days
Secondary Outcome Measure Information:
Title
Percentage of patients with PaO2 to Fi02 ratio > 300
Description
Mean every 48 hours PaO2 to FiO2 ratio
Time Frame
7 days
Title
Lengths of hospital-stay
Description
To compare the lengths of hospital-stay
Time Frame
Days 60
Title
Mortality rate
Description
All cause mortality
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Persons over 18 years of age of any sex admitted with a diagnosis of a suspected case of COVID-19, in accordance with the definition of the Ministry of Health of the Nation (MSal) as of May 20, 2020, who present at the time of admission or in its evolution pulmonary infiltrates compatible with imaging studies (chest X-ray or chest CT) and at least one of the following biochemical parameters of systemic inflammation: D DIMER over 1.0 ug/dl Ferritin over 500 ng/ml Fibrinogen over 500 mg/dl Exclusion Criteria: Under 18 years old Pregnant women Known allergy to Heparin Participant in another clinical trial that is not approved for joint enrollment. APTT> 120 seconds, not due to anticoagulant therapy. Platelet count <20 x 109 per L Lung bleeding. Uncontrolled bleeding Advanced neurological impairment Advanced oncological disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
ALICIA B VILASECA, DR
Phone
+5401148588144
Ext
244
Email
avilaseca@clinicasancamilo.org.ar
First Name & Middle Initial & Last Name or Official Title & Degree
Ruben F Barbera, DR
Phone
+5401148588199
Email
rbarbera@clinicasancamilo.org.ar
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
ALICIA B VILASECA, DR
Organizational Affiliation
CLINICA SAN CAMILO
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinica San Camilo
City
Ciudad Autonoma de Buenos Aire
State/Province
Buenos Aires
ZIP/Postal Code
1405
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ALICIA B VILASECA, DR
Phone
+54 91160993060
Email
avilaseca@gmail.com
First Name & Middle Initial & Last Name & Degree
RUBEN F BARBERA, DR
Phone
+541148588198
Email
RBARBERA@CLINICASANCAMILO.ORG.AR

12. IPD Sharing Statement

Plan to Share IPD
No
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Nebulized Heparin in Severe Acute Respiratory Syndrome COVID-19

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