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This other clinical trial compares robot-assisted US scanning with handheld US scanning and ground-truth CT data of the lumbar spine in healthy, young volunteers. The main questions it aims to answer are:
Participants will:
Full description
The following hypotheses are tested:
The project consists of three pillars as objectives to help solidify the US reconstruction of the lumbar spine as a novel navigational method in interventional spine applications.
This project consists of two phases. First, a preliminary pilot study is planned to assess the project's feasibility and improve the planned workflow and safety measures. For this pilot, the investigators will mouth-to-mouth recruit two volunteers. After completing and thoroughly evaluating the pilot, the investigators will conduct the actual study.
The volunteers for the actual study are selected through public calls for participation. Possible volunteers are young, healthy, and not affected by illness or deformation of the lumbar spine. The selected volunteers are screened by asking about their medical history. If included and willing to participate, the volunteers are invited to the study at Balgrist Campus and will be clinically examined regarding the lumbar spine. Furthermore, a low-dose CT scan, a handheld US scan, and a robot-assisted US scan are held.
The CT scans are manually segmented into 3D surface models to obtain a "segmentation ground truth". A novel machine learning algorithm automatically performs 3D reconstruction and segments the robot-assisted and handheld US scans.
The 3D US reconstructions are then utilized to identify pedicle screw trajectories through a novel method based on the posterior anatomical landmarks of lumbar vertebrae.
This single-center study combines the clinical and computer-science knowledge from the Research in Orthopedic Computer Science (ROCS) team of the University of Zurich, Switzerland, with the robotics and US application knowledge from the Faculty of Engineering of the University of Leuven, Belgium. The data collection is performed at Balgrist Campus.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Documented volunteer refusal
Volunteers in whom CT cannot be performed
Positive pregnancy test prior to radiology (contraindication to CT)
Pregnancy
Chronic pain in the lumbar spine
Moderate or severe deformity of the lumbar spine
Any prior intervention to the lumbar spine:
Fracture of the lumbar spine
BMI below 19 kg/m2 or above 25 kg/m2
Anatomies, such as subcutaneous fat or tendon, occlude the bony surface or do not allow a clear image in the US scan
Primary purpose
Allocation
Interventional model
Masking
63 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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