C. Work performed during Period 3
Demonstrator Device
A Demonstrator has been made based on the experience from a first version demonstrator device and the outcome of an earlier conducted user study.
The Demonstrator device consists of two handpiece half parts, which may be used in a connected state to measure local carotid pulse wave velocity or as separate units to measure carotid-femoral pulse wave velocity, arterial stenosis (only one handpiece half part) and cardiac contraction patterns (only one handpiece halfpart). The two handpiece half parts are tethered to an external data acquisition rack system.
The Demonstrator device has been developed, validated and released for use in a clinical feasibility study setting. As a part of the development, a risk analysis and risk mitigation process has been conducted to assure safety of the patient as well as the operator.
The demonstrator device has successfully been used in the planned clinical feasibility studies.
Biomechanical modelling
3D Computational Fluid Dynamics (CFD) simulations, resolving the flow turbulences induced by a stenosis, were performed to assess the impact of the grade of stenosis and trans-stenotic carotid flow. Simulations indicated that moderate to severe stenosis can be detected from the analysis of the power spectrum in the 50-200 Hz frequency band. These findings were confirmed by hydraulic bench simulations.
In parallel with the computational and experimental work, software was developed for the automated off-line processing of multi-beam LDV data obtained with demonstrators 1 and 2, mainly focusing on measurement of local carotid PWV. The skin acceleration, rather than displacement or velocity, was identified as the signal most suited for further processing. A data set of 100 subjects, collected at HEGP in Paris, was analyzed, yielding plausible values of local PWV in all subjects.
Clinical feasibility trials
A PWV pilot clinical study has been conducted at George Pompidou Hospital (INSERM Paris) collecting a substantial clinical dataset, 100 both from healthy subjects as well as from patients with cardiovascular conditions. The quality of the CARDIS device readings was found to be very good. Also, the measurement data and variability within sessions were in line with reference techniques showing a clear correlation.
Another clinical study was being conducted at Maastricht University Hospital to assess the capability of the CARDIS prototype to assess cardiac dyssynchrony, a parameter related to hear failure occurrence, and the preliminary results showed also a consistent accordance between the gold standard and the investigational device from this project.