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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. €

0

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.

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

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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