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Anticoagulation in Patients Suffering From COVID-19 Disease The ANTI-CO Trial

Primary Purpose

Anticoagulation in COVID-19 ARDS

Status
Unknown status
Phase
Phase 4
Locations
Qatar
Study Type
Interventional
Intervention
Bivalirudin Injection
Standard treatment
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Anticoagulation in COVID-19 ARDS focused on measuring COVID-19, ARDS, Anticoagulation

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patient (≥ 18 years of age)
  • Positive COVID-test
  • Under mechanical ventilation
  • D-Dimers>1.2 mg/L

Exclusion Criteria:

  • Pregnancy
  • Allergy to the drug (bivalirudin)
  • Inherited coagulation abnormalities
  • No informed consent

Sites / Locations

  • Hamad Medical CorporationRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard treatment

Bivalirudin arm

Arm Description

In this arm the patients will be treated according to our standard anticoagulation protocol. The patients will not be treated with Bivalirudin (the investigational drug).

The patients will be anticoagulated according to the institutional HIT-protocol which uses Bivalirudin as anticoagulant.

Outcomes

Primary Outcome Measures

P/F ratio
the P/F ratio is a surrogate parameter for oxygenation in ARDS.

Secondary Outcome Measures

Kidney function
The kidney function frequently is deteriorated in COVID-19 patients

Full Information

First Posted
June 23, 2020
Last Updated
June 23, 2020
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT04445935
Brief Title
Anticoagulation in Patients Suffering From COVID-19 Disease The ANTI-CO Trial
Official Title
Anticoagulation in Patients Suffering From COVID-19 Disease-The Anti-Co Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 28, 2020 (Anticipated)
Primary Completion Date
September 28, 2020 (Anticipated)
Study Completion Date
March 28, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hamad Medical Corporation

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
Patients with COVID-19 associated ARDS and mechanical ventilation have a high mortality. Part of the disease is an activation of the coagulation system which seems to contribute to clotformation in the pulmonary bloodstream. Recently we implemented an algorithm applying higher doses of heparins (LMWH). However, this approach could not inhibit clotformation enough. Bivalirudin could prevent clotformation better and support dissolving existing clots. Therefore, we want to compare 50 patients with the standard treatment with 50 patients under bivalirudin treatment which we normally apply in patients with a HIT-syndrome. Our primary outcome measure is oxygenation reflected as P/F ratio.
Detailed Description
The pandemic of COVID-19, a newly upcoming viral disease caused by SARS-CoV-2, puts the whole worlds health system under pressure. Patients suffering from this disease mainly develop respiratory symptoms, which can lead to severe acute respiratory distress syndrome (ARDS) necessitating ICU admission in 10-20% of the cases admitted to hospital. In addition to these symptoms, patients show lymphopenia, cardiac symptoms and altered coagulation profiles. Although those patients are treated in the ICU the mortality there is more than 20% due to multiorgan failure. One of the recent insights in this disease is its effect on the coagulation system. Meanwhile we know that the coagulation system gets activated. Furthermore, it seems that clot formation takes place in the pulmonary micro-vasculature which could contribute to the widely observed gas-exchange impairment. Therefore, many centers apply empiric anticoagulation for their COVID-patients. At the moment, we at HMC, also apply an empirical anticoagulation protocol as our standard approach. However, this is a symptomatic treatment without good proof. Bivalirudin is a well-known agent which is used in HMC for cases in which anticoagulation is needed, but a contraindication for heparin exists (i.e. HIT syndrome). This drug has an interesting pharmacologic profile. It acts independent of antithrombin (AT), the physiological compound which enhances heparin effects under normal circumstances. This lack of dependence on AT, makes Bivalirudin an attractive choice in light of the contradictory reports on the levels of AT during COVID infection. If AT levels are decreased during the infection, heparin (as well as LMWH) cannot work efficiently, which would render our treatment less effective. Luckily, bivalirudin acts without the support of AT, so we could bypass this problem. In addition, bivalirudin has some fibrinolytic activities. It inhibits clot-bound thrombin which as a result destabilizes the clot rendering it more susceptible to thrombolysis. This property partially supports the dissolving of clots and could support re-opening the pulmonary microcirculation. Objectives: To prove the positive effect of anticoagulation with bivalirudin intravenously on gas-exchange in patients with COVID-19 and respiratory failure on invasive mechanical ventilation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anticoagulation in COVID-19 ARDS
Keywords
COVID-19, ARDS, Anticoagulation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized controlled trial.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
This study will be blinded to the above mentioned group. The PI is not involved in active treatment. Patients are sedated and ventilated when treatment starts and finally the outcome assessors will not be knowing the patients treatment.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard treatment
Arm Type
Active Comparator
Arm Description
In this arm the patients will be treated according to our standard anticoagulation protocol. The patients will not be treated with Bivalirudin (the investigational drug).
Arm Title
Bivalirudin arm
Arm Type
Experimental
Arm Description
The patients will be anticoagulated according to the institutional HIT-protocol which uses Bivalirudin as anticoagulant.
Intervention Type
Drug
Intervention Name(s)
Bivalirudin Injection
Other Intervention Name(s)
anticoagulation
Intervention Description
The patients will receive iv Bivalirudin according to the institutional HIT protocol.
Intervention Type
Drug
Intervention Name(s)
Standard treatment
Intervention Description
This group will receive standard anticoagulation with LMWH/UFH
Primary Outcome Measure Information:
Title
P/F ratio
Description
the P/F ratio is a surrogate parameter for oxygenation in ARDS.
Time Frame
three days of intervention
Secondary Outcome Measure Information:
Title
Kidney function
Description
The kidney function frequently is deteriorated in COVID-19 patients
Time Frame
three days of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patient (≥ 18 years of age) Positive COVID-test Under mechanical ventilation D-Dimers>1.2 mg/L Exclusion Criteria: Pregnancy Allergy to the drug (bivalirudin) Inherited coagulation abnormalities No informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marcus Lance, MD, PhD
Phone
00974
Ext
33530292
Email
mlance@hamad.qa
First Name & Middle Initial & Last Name or Official Title & Degree
Stefan Roehrig, MD, MBA
Phone
00974
Ext
66030924
Email
srohrig@hamad.qa
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcus Lance, MD, PhD
Organizational Affiliation
HMC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamad Medical Corporation
City
Doha
Country
Qatar
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nadir Kharma, MD
Phone
00974
Ext
55118621
Email
nkharma@hamad.qa

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
this will depend on IRB advice
Citations:
PubMed Identifier
35244208
Citation
Flumignan RL, Civile VT, Tinoco JDS, Pascoal PI, Areias LL, Matar CF, Tendal B, Trevisani VF, Atallah AN, Nakano LC. Anticoagulants for people hospitalised with COVID-19. Cochrane Database Syst Rev. 2022 Mar 4;3(3):CD013739. doi: 10.1002/14651858.CD013739.pub2.
Results Reference
derived
PubMed Identifier
32895056
Citation
Kharma N, Roehrig S, Shible AA, Elshafei MS, Osman D, Elsaid IM, Mustafa SF, Aldabi A, Smain OAM, Lance MD. Anticoagulation in critically ill patients on mechanical ventilation suffering from COVID-19 disease, The ANTI-CO trial: A structured summary of a study protocol for a randomised controlled trial. Trials. 2020 Sep 7;21(1):769. doi: 10.1186/s13063-020-04689-1.
Results Reference
derived

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Anticoagulation in Patients Suffering From COVID-19 Disease The ANTI-CO Trial

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