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ClearRing

An innovative, minimally invasive medical device used for treatment of Benign Prostatic Hyperplasia symptoms.

Total Cost €

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EC-Contrib. €

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Partnership

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 ClearRing project word cloud

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

feasibility    easily    normal    time    ineffective    urgent    25    bladder    supply    twice    iso    daily    tolerable    there    therapy    13845    invasive    sufferers    alpha    surgery    frequency    market    approximately    urination    severity    blockers    minimally    moderate    benign    infertility    transurethral    operation    strategy    extraneous    treatment    ce    potentially    resection    chain    harsh    fast    million    removed    device    clinical    introducing    headaches    active    stream    severe    standard    men    mark    costly    plan    drafted    optimize    gold    located    trial    elongated    lifestyle    dysfunction    worldwide    procedure    tools    patients    safe    starting    alternative    reduce    relief    symptoms    designed    weakness    shaft    inserted    lifestyles    clearring    prostate    advantage    pro    surgeons    erectile    disrupt    arc    hospitals    initiated    bph    housing    irritability    innovation    urinate    difficulty    resume    turp    dizziness    medical    weak    prostatic    drugs    unmet    expand    hyperplasia    patient    obtain    implants    upgrade   

Project "ClearRing" data sheet

The following table provides information about the project.

Coordinator
PROARC MEDICAL LTD 

Organization address
address: KIDMA 23
city: PARDES HANA
postcode: 3707923
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 http://proarcmedical.com/
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.3.1.4. (Active ageing and self-management of health)
2. H2020-EU.2.1.1. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies - Information and Communication Technologies (ICT))
3. H2020-EU.2.3.1. (Mainstreaming SME support, especially through a dedicated instrument)
4. H2020-EU.3.1.6. (Health care provision and integrated care)
 Code Call H2020-SMEINST-1-2016-2017
 Funding Scheme SME-1
 Starting year 2018
 Duration (year-month-day) from 2018-01-01   to  2018-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    PROARC MEDICAL LTD IL (PARDES HANA) coordinator 50˙000.00

Map

 Project objective

There are approximately 30 million men worldwide who experience moderate to severe Benign Prostatic Hyperplasia (BPH) symptoms. These symptoms, such as urgent need to urinate, difficulty starting urination, weak stream, or increased frequency of urination, are severe enough to disrupt a patient’s daily lifestyle. Of the 30 million sufferers, an estimated 25% require immediate active treatment. Transurethral Resection of the Prostate (TURP), the current gold standard procedure, is costly, ineffective, and can lead to harsh side effects such as infertility, erectile dysfunction, and bladder irritability, while alpha blockers can lead to weakness, dizziness, and headaches. Therefore, there is a significant unmet need for minimally invasive BPH therapy as a less costly, tolerable, and safe alternative to drugs and surgery. Pro Arc Medical is introducing the ClearRing system, designed to expand the prostate and provide immediate relief of BPH symptoms. Because all of the tools necessary are located within the housing of the elongated shaft, the device can easily be inserted and removed without the need for extraneous procedures. The ClearRing system will bring an immediate cost reduction and time advantage to surgeons and hospitals. The minimally invasive procedure will reduce the range and severity of side effects allowing patients to resume their normal lifestyles potentially twice as fast as the current standard operation procedure. During the feasibility assessment, a go-to-market strategy and a supply chain will be established, as well as further development plan will be drafted. Pro Arc will upgrade the ClearRing system, as well as optimize the system in order to allow for two implants to be inserted at the same time during the second phase of innovation project. A clinical trial will then be initiated to obtain ISO 13845 and CE mark.

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

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