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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.

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

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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