A small, portable cold plasma device for the treatment of chronic and acute wounds.

Informazioni relative al progetto

plasmaCare

ID dell’accordo di sovvenzione: 816023

DOI

10.3030/816023

Progetto chiuso

Data della firma CE 20 Giugno 2018

Data di avvio 1 Luglio 2018

Data di completamento 31 Ottobre 2018

Finanziato da

• INDUSTRIAL LEADERSHIP - Innovation In SMEs

Costo totale

€ 71 429,00

Contributo UE

€ 50 000,00

Coordinato da

TERRAPLASMA GMBH
Germany

Periodic Reporting for period 1 - plasmaCare (A small, portable cold plasma device for the treatment of chronic and acute wounds.)

Periodo di rendicontazione: 2018-07-01 al 2018-10-31

Sintesi del contesto e degli obiettivi generali del progetto

The overall objective of the feasibility study was to analyse the opportunities that lie in our cold atmospheric plasma technology for the treatment of skin wounds, as well as the commercial opportunities that follow such a development.
At Terraplasma we have developed a technology for for the treatment of wounds based on cold atmospheric plasma device and we are currently exploring further applications of the device for the home treatment of skin diseases of bacterial origin (i.e. acne) and/or minor acute wounds

Lavoro eseguito dall’inizio del progetto fino alla fine del periodo coperto dalla relazione e principali risultati finora ottenuti

terraplasma has completed a full analysis of the technical and business potential of the plasma care home device. Throughout this project, we have greatly expanded our knowledge regarding the clinical validation and regulatory approval required for a European market launch of the plasma care home. Furthermore, terraplasma has defined the remaining optimisation and upgrade activities required for the components of the plasma care home system and the involvement of of a contract manufacturer for the device line of production. We acknowledged that according to the current regulations, a pre-clinical validation conducted with the partnership of the Universitätsklinikum Regensburg as well as a clinical evaluation including an equivalence consideration with the professional plasma care© device would be sufficient to apply for the CE Mark.
The pre-clinical validation was defined with the key objective of demonstrating the usability of the device, to treat acne and improve acne scar healing successfully using the plasma care home device, and to demonstrate the safety of the medical device for home and self-usage. Following the obtained results, terraplasma will submit the necessary technical documentation for approval and CE Marking. In addition, we analysed the go-to-market strategy to define the approach for an effective market uptake and we started talking with 2 major medical device distributors in Europe and the US that showed interest in the forthcoming commercialization of a cold plasma device for acne treatment.

Progressi oltre lo stato dell’arte e potenziale impatto previsto (incluso l’impatto socioeconomico e le implicazioni sociali più ampie del progetto fino ad ora)

The cold plasma technology incorporates a plasma source, which produces many millions of controlled micro-discharges, which in turn ionize the surrounding air locally and thus generate a non-equilibrium chemistry which produces a reactive mix of plasma species, which are identical to those produced by the human innate immune system in its fight against infections. We have applied the innovative cold atmospheric plasma technology to treat acute and chronic wounds in the hospital care, in an efficient and cost-effective way. The next challenge is be to apply the technology to a consumer device for the treatment of acne and minor acute wounds for use at home

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