ICM+ was found to be versatile and robust enough to be employed as the main data collection tool in multi-centre clinical trials. With the new ICM+ Clinical Trial Assistant, it is possible to configure the software to aid in the execution of clinical trials.
CENTER-TBI is a large European project that aims to improve care for patients with Traumatic Brain Injury (TBI). In this project, ICM+ was the cornerstone of the high-resolution sub-study where it served as the main data collection system used in 20 centres all over Europe.
During the study, 250+ patients were recruited for high-resolution monitoring with a total recording time of more than 1,700 days.
Despite the innate differences throughout all the participating centres, be it in different work methods and monitoring devices, ICM+ was capable of successfully gathering all the data in a robust and homogeneous way.
This is a feasibility study that aims to test the use of the CPPopt-guided therapy prospectively in clinical practice (trial link). The study will be conducted in 3 centres: Cambridge, Leuven, and Maastricht.
This will be the first time that the new Clinical Trial Assistant will be put to use.
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In order to activate the assistant you need to select the project that was configured to load the assistant module for a specific clinical trial -
Example of the Clinical Trial assistant allowing the user to select the arm in which the patitent was randomized. -
Example of a question asked by the assistant to the user. All of the data inserted through the assistant isstored in the ICM+ session file