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Measuring Force During Subpial Resection Procedure Using a Novel Ex Vivo Calf Brain Model With Integrated Sensor

12 de agosto de 2026 actualizado por: Rolando Del Maestro, McGill University

Neurosurgery is a high-stakes surgical specialty where errors can result in significant morbidity. The amount of force applied simultaneously on the brain with multiple different instruments during complex neurosurgical procedures is a critical safety metric that, to the investigators' knowledge, has not been previously measured in a realistic operative environment.

The investigators have therefore developed a simulation platform integrating an ex vivo calf brain and a 3D-printed skull model attached to a force sensor capable of capturing real-time forces applied to the brain. A case series study will be conducted to evaluate the pattern of force applied. Medical students, neurosurgical residents, and staff neurosurgeons from McGill University will be recruited to perform subpial resections using our ex vivo calf brain simulation platform. The forces applied by the microscissors, bipolar forceps, and ultrasonic aspirator onto the brain will be captured. This study aims to demonstrate the spectrum of force applied during a neurosurgical procedure using an ex vivo calf brain model.

Descripción general del estudio

Estado

Terminado

Descripción detallada

Background and Rationale: The subpial resection technique is a complex neurosurgical procedure that is essential for brain tumor and epilepsy surgery. However, opportunities for trainees to gain hands-on experience with this procedure without risk to patient safety are limited. The force applied on the brain during tool-tissue contact is a critical factor impacting patient safety. While virtual simulation platforms enable force monitoring, ex vivo animal brains cannot readily capture quantitative data. The investigators have therefore developed a prototype of a simulation platform that integrates a force sensor and a calf brain and can accurately detect real-time forces during simulated subpial resections. This study seeks to gauge the force spectrum using this ex vivo calf brain force detection system.

Hypothesis: The simulation platform will accurately measure forces applied by novice, intermediate, and expert participants with surgical instruments on an ex vivo calf brain during simulated subpial resection procedures.

Co-Primary Outcomes: To assess the individual and combined instrumental force applications during subpial resection procedures in an ex vivo calf brain model.

Secondary Outcome: To differentiate levels of expertise of trial participants.

Setting: Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Participants:

Neurosurgeons (experts): Staff neurosurgeons at McGill University specializing in oncology, epilepsy, pediatric, or vascular neurosurgery

Neurosurgical residents (trainees): Neurosurgical residents at McGill University

Medical students (novices): Students enrolled in medical school at McGill University

Design: A cross-sectional case series study.

Methodology: This study was approved by the McGill University Health Centre Research Ethics Board, Neurosciences-Psychiatry. A case series study will be conducted where medical students, neurosurgical residents, and staff neurosurgeons from McGill University will be recruited to perform subpial resection tasks on an ex vivo calf brain model. Calf brains will be placed in a 3D-printed skull model to mimic a realistic human operative environment. The 3D-printed skull model was prototyped from a publicly available CT scan obtained from Embodi3D, an open-access medical imaging repository, and reconstructed in 3D using the open-source software 3D Slicer version 5.10.0. A 6-degree-of-freedom force/torque sensor (Nano17 IP68, ATI Industrial Automation Inc., North Carolina, USA) and a USB data acquisition board (NI-6210, National Instruments Inc., Texas, USA) will be used to measure real-time forces applied to the brain. Participants will use microscissors, bipolar forceps, and a SONOPET ultrasonic aspirator (Stryker, Portage, Michigan, USA) to perform simulated procedures. The tasks will be performed using an OPMI pico surgical microscope (ZEISS, Jena, Germany) and video-recorded using a Blackfly S GigE embedded microscope camera (FLIR, Wilsonville, Oregon, USA), allowing a broader instrument view for evaluation of intraoperative and postoperative performance.

Study Procedure: Upon arrival, participants will read and sign an informed consent form. They will then fill out a pre-trial questionnaire assessing their demographic characteristics (e.g., sex, gender, age, institutional affiliation, etc.). Each participant will receive standardized instructions on instrument use and function and be presented with an image outlining the location of pial cuts and the subpial resections on the ex vivo calf brain in front of them. Participants will adjust the operating microscope according to their preferences. The subpial resection experiment will be divided into three subsequent tasks. The goal is to obtain a noise-free and specific force measurement for each of the major instruments/maneuvers in a standard subpial resection. The first task entails using microscissors to create a 2-cm pial cut in ten different gyri across a calf brain hemisphere (n = 10). The time allocated for this task is 30 seconds for each cut. The second task involves utilizing bipolar forceps to grasp and lift the edge of the pia where cuts are made with the microscissors in task 1. A repetitive lift and hold maneuver will be repeated five times assuming a right to left direction across the pial incision line in 5-second intervals using the left hand. This will be repeated across each of the ten different pial cuts (n = 50). The time allocated for this task is maximum of one minute for each pial defect. Finally, an ultrasonic aspirator in the dominant (right) hand along with the bipolar in the opposite hand will be employed to perform subpial resection at three out of the ten pial cuts originally made in task 1 (n = 3). Each of the three spots would undergo subpial resection for an allocated time of 3 minutes across separate recordings.

Significance: This study will provide the first insights into a realistic operative environment where it will be possible to monitor the force applied on the brain.

Tipo de estudio

De observación

Inscripción (Actual)

11

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Quebec
      • Montreal, Quebec, Canadá, H3A 2B4
        • Neuro Imaging and Surgical Technologies Lab, Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Método de muestreo

Muestra no probabilística

Población de estudio

Staff neurosurgeons, neurosurgical residents, and medical students from McGill University

Descripción

Inclusion Criteria:

  • Right-handed medical students, neurosurgical residents, and staff neurosurgeons from McGill University

Exclusion Criteria:

  • Left-handed individuals

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Forces applied to the brain during each simulated subpial resection procedure step
Periodo de tiempo: 1 day of study
Throughout each simulated ex vivo subpial resection procedure, forces applied to the brain during tool-tissue contact will be measured by the force/torque sensor in grams and Newtons.
1 day of study

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Rolando F. Del Maestro, MD, PhD, Neurosurgical Simulation and Artificial Intelligence Learning Centre, McGill University
  • Director de estudio: Amir Hooshiar, PhD, Surgical Performance Enhancement and Robotics Centre, McGill University
  • Director de estudio: D. Louis Collins, PhD, Neuro Imaging and Surgical Technologies Lab, McGill University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

3 de junio de 2026

Finalización primaria (Actual)

8 de julio de 2026

Finalización del estudio (Actual)

8 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

10 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

10 de junio de 2026

Publicado por primera vez (Actual)

16 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

14 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

12 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2018 4395, Trial 1

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • CÓDIGO_ANALÍTICO
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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