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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.

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

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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