Periodic Reporting for period 5 - CIRDinnova (Shifting the limits of resuscitation with “CIRD Controlled Integrated Resuscitation Device”)
Okres sprawozdawczy: 2021-12-01 do 2022-05-31
The overall rationale of the CARL therapy is to minimize reperfusion injury combined with a replenishment of substrates and energy in the cells in order to support the consequent repair processes. This therapeutic strategy is based on two main features: (a) the adaption of the chemical composition of the reperfusion solution by pharmaceuticals, and (b) the control of the physical conditions of reperfusion i.e. flow, pressure, temperature etc. Core of the therapeutic approach is the measurement of a set of biomarkers in a real-time fashion in order to take immediate therapeutic measures by administering of pharmaceuticals. The fast controlled and automated adaption of the chemical and physical parameters during the treatment is a completely new approach in the field of cardiopulmonary resuscitation.
This unique combination of innovative therapy and medical device represents a highly promising market opportunity: the CARL therapy can only be performed with the CARL System which can only be delivered by Resuscitec. The CARL system is a specific device for the extra-corporeal circulation of blood (a special kind of heart-lung-machine) specifically designed to apply the new CARL therapy. As most of the resuscitations take place out of hospital has been designed as a mobile system which can be transported to any place where patients suffer from a cardiac arrest.
The CARL technology is protected by patents in the ownership of Resuscitec. The overall objective of the innovation action which brings together three clinical partners with the manufacturer of the CARL system device is to achieve market readiness with respect to all relevant aspects and conditions to realise a fast and economic successful market entry and uptake in the year 2022 and to show European leadership in the field of emergency medicine and resuscitation devices. That means especially to achieve clinical market readiness beyond the regulatory market approval in a real world system validation to show extended clinical evidence, safety and efficacy of CARL. Besides this it will be essential to achieve user qualification readiness by developing tools and training programmes for users and proctors for a safe, sustainable and successful deployment and dissemination of CARL.