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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.

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

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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