Several progresses beyond the state of the art were achieved: new methods for 3D US acquisition and reconstruction, real-time methods for multimodal image registration, new methods for the calibration of the deformable models and compensation of the deformations, prototypes of a robotic head for breast and muscle biopsies, new methods for the control of a robotic arm to perform the 3D US scanning of a soft tissue, identification of materials for the realization of multimodal markers, a new pad sensor to be attached to the US probe for elastography measurements. A new method for interactive scanning has been developed (SLAM) including the use of image feedback on robotic scanning.
Some of these realizations may become commercial products by themselves (e.g. multimodal markers, image acquisition system, US pressure sensor).
Most of the technologies developed so far were integrated in the MURAB robotic system and tested on realistic phantoms of the breast and of the leg. Subparts were tested in-vivo. The consortium prepared the hardware and software for clinical trials and the for the approval required by the ethical committee, however it was not possible to finalise the clinical testing due to the outbreak of the COVID-19 pandemic. A complete analysis of the market and of the business model was performed by Siemens. This analysis comprised studies about: potential markets, market size, costs of the MURAB procedure and comparison with the cost of a standard procedure, number of MRI guided biopsies in the countries involved in the consortium and the potential number of MURAB installations within a country.
Also, the possibility to extend the MURAB system to other cases (e.g. liver, kidneys) may lead to a major socio-economic impact of the project.