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The purpose of this study is to evaluate the accuracy of the Neurolocate recording system of the neurosurgical robot Neuromate, marketed by Renishaw, in order to optimize surgical procedures, costs and patient comfort.
Robotic neurosurgery has been developed for nearly 25 years and offers neurosurgeons many advantages, including increased precision. Accuracy is a key point for stereotactic neurosurgical procedures, particularly for deep brain stimulation electrode implantations. The accuracy of the Neuromate robot was measured in stereotactic framed and frameless mode in vitro and in vivo during stereo-electroencephalography procedures. Investigators also evaluated the actual accuracy of its application in routine deep brain stimulation procedures using a measurement system independent of the robot itself and the manufacturer. We showed that the average in vivo accuracy was 0.86 mm and the maximum error was 1.55 mm. This accuracy is at least similar to the accuracy of stereotactic frame arms and is compatible with the accuracy required in deep brain stimulation procedures. The Neurolocate device is a new non-invasive, frameless patient matching module designed for use with the Neuromate stereotactic robot. The main advantages of the Neurolocate system are that it is less invasive than screw-on markers, simplifies the surgical procedure and reduces the duration of the surgery The accuracy of the Neurolocate frameless recording system was evaluated in vitro and in vivo for robotic stereo-electroencephalography trajectories in epileptic patients and compared to the accuracy of conventional recording using a stereotactic frame. However, the accuracy of the Neurolocate recording system has never been measured in vivo during deep brain stimulation procedures.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Department of neurosurgery
Nice, France
Start Date
January 26, 2021
Primary Completion Date
January 7, 2022
Completion Date
January 7, 2023
Last Updated
June 12, 2023
18
ACTUAL participants
deep brain stimulation
PROCEDURE
Lead Sponsor
Centre Hospitalier Universitaire de Nice
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06692920