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  • Periodic Reporting for period 1 - ISSD (The Implantable Subcutaneous String Defibrillator, an innovative subcutaneous cardioverterdefibrillator for a new paradigm in cardiac rhythm management.)
H2020

ISSD Report Summary

Project ID: 790070

Periodic Reporting for period 1 - ISSD (The Implantable Subcutaneous String Defibrillator, an innovative subcutaneous cardioverterdefibrillator for a new paradigm in cardiac rhythm management.)

Reporting period: 2017-11-01 to 2018-02-28

Summary of the context and overall objectives of the project

Sudden Cardiac Arrest (SCA) is a life-threatening heart condition and one of the most common causes of death in developed countries. It claims more than 350,000 lives per annum in Europe1 and about 95% of people who have SCA die before they reach the hospital. Ventricular Fibrillation is the major cause of SCA and the only effective treatment for it is to prompt electrical defibrillation. There are currently two different implantable technologies to prevent SCAs: 1) Transvenous Implantable Cardioverter-Defibrillators (TV-ICDs), which are implanted under the skin with leads that snake through veins into the heart and are attached to the heart ventricles or atria; and 2) Subcutaneous Implantable Cardioverter-Defibrillators (S-ICD), which also have generators and leads but avoiding leads within the heart, being implanted subcutaneously in whole with no leads within the heart. However, each of these technologies are mired with problems including patient discomfort and as in the case of the S-ICD, a big surgical pocket at implant, and negative impact due to the ICD relatively large generator´s size, the need to replace their batteries every 5-7 years which requires a new replacement operation as well as use of intensive fluoroscopy with occasional lead extractions. NewPace has developed the Implantable Subcutaneous String Defibrillator (ISSD), to address the need for better patient outcomes due to SCA, providing more reliable and safe cardiac rhythm management. The overall objectives of the project are to complete development of the ISSD device, undertaking a series of preclinical tests to confirm its safety and effectiveness, and eventually validating it through a clinical trial with European medical centres. Completion of these objectives will result in a product that is ready for the market.

Work performed from the beginning of the project to the end of the period covered by the report and main results achieved so far

During Phase 1, NewPace produced a work plan, detailing the main technical steps to make ISSD ready for market. Also during the Feasibility Study, the business viability has been evaluated by means of a detailed market analysis (size, barriers, customer segments, competitors) and preparing a commercialisation strategy and a detailed financial analysis to understand the expected financial performance. The results achieved during the project, confirming the products expected performance by all stakeholders will be communicated through a series of communication channels (online, events such as conferences, publications). For patients, the device is expected to result in an improved quality of life. The adoption of ISSD should also lead to savings in the healthcare sector thanks to less complications post-operation and fewer replacements needed, and reduced risk of infection.

Progress beyond the state of the art and expected potential impact (including the socio-economic impact and the wider societal implications of the project so far)

The ISSD will provide the following key benefits: (1) Subcutaneous: implanted subcutaneously with no leads within the heart; (2) Unitary and flexible: totally integrated (no can, nor leads) and flexible string shape device; (3) Rechargeable: requires one hour/once in a year wireless recharge, designed for 10 years before replacement; (4) Smart phone connectivity: low energy Bluetooth communication (BLE) providing remote monitoring functionalities using a simple smart phone app.

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