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ViaOne

A MINIMALLY INVASIVE NEEDLE FREE DEVICE TO SAFELY ACCESS THE PERICARDIUM SPACE

Total Cost €

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EC-Contrib. €

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Partnership

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 ViaOne project word cloud

Explore the words cloud of the ViaOne project. It provides you a very rough idea of what is the project "ViaOne" about.

medical    competitive    needles    workspace    motion    ensures    af       surgery    cardiac    procedure    constant    opportunity    heart    patients    fact    confident    24m    device    failed    people    600m    pathological    requiring    complications    tools    epiviasystem    thread    acute    secure    250    outcomes    variety    free    skill    tamponade    equivalent    catheters    cardiovascular    first    additional    ablation    30    expertise    pericardium    atrial    arrhythmia    fibrillation    clinical    il2018    safe    pathologies    big    financial    130    commercialize    performed    optimize    market    release    treatment    5m    penetration    050670    avoiding    mapping    healthcare    manner    sme    employs    structured    epicardial    11m    needle    disorders    ablations    commercial    patient    representing    marketable    space    geometrically    deaths    techniques    area    puncture    2016    business    price    reduce    pericardial    feasibility    successful    electrohpysiological    bleeding    invasive    2021    pct   

Project "ViaOne" data sheet

The following table provides information about the project.

Coordinator
CARDIOVIA LTD. 

Organization address
address: WADI EL HAJ 13
city: NAZARETH
postcode: 1600101
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Israel [IL]
 Project website https://www.cardiovia.com/
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.3. (PRIORITY 'Societal challenges)
2. H2020-EU.2.3. (INDUSTRIAL LEADERSHIP - Innovation In SMEs)
3. H2020-EU.2.1. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies)
 Code Call H2020-SMEInst-2018-2020-1
 Funding Scheme SME-1
 Starting year 2019
 Duration (year-month-day) from 2019-05-01   to  2019-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CARDIOVIA LTD. IL (NAZARETH) coordinator 50˙000.00

Map

 Project objective

2.5M patients per year in the US and the EU require pericardial space access as the result of a variety of pathological conditions. Atrial Fibrillation (AF) is the most common condition requiring pericardial access, in fact, AF affected 24M people in the US and 11M in the EU (2016). In current epicardial access techniques (using needles), complications can reach 4.5-30% (representing a Ëž€600M/year increase in costs for healthcare systems) and includes heart puncture, cardiac tamponade and pericardial bleeding, which can result in an increase in patient deaths. The use of a needle in the heart area, which is in constant motion, requires a high level of skill and expertise during surgery. EpiVIASYSTEM is the first device (PCT /IL2018 /050670) to ensure pericardial access in a confident, safe, needle-free manner avoiding complications during penetration of the pericardium. The device employs a unique geometrically structured thread that ensures a secure workspace for the use of additional cardiovascular devices, such as mapping and ablation catheters for treatment of arrhythmia disorders. Its design will ensure a competitive price of €250/procedure when compared with €130 for the equivalent tools used in invasive non-electrohpysiological procedures. EpiVIASYSTEM is expected to improve clinical outcomes of patients and reduce costs associated with failed ablations associated with the needle use by €600M/year. The increased growth of cardiac pathologies and the 2.5M of patients/year that require pericardial access represent a big business opportunity for the EpiVIASYSTEM and will favour its successful market uptake. EpiVIASYSTEM´s main objective is to optimize, scale-up and commercialize a marketable medical device in both the EU and the US by 2021. For that, a feasibility study will be performed during SME Phase 1 to evaluate any technical, commercial and/or financial issues and ensure the successful release of the EpiVIASYSTEM into the market.

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The information about "VIAONE" are provided by the European Opendata Portal: CORDIS opendata.

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