Healthy Clinical Trial
Official title:
Robot-Assisted US-Based Vertebral Segmentation for Pedicle Screw Trajectory Identification: A Comparison With Handheld US-Reconstructions and Ground Truth CT-Data
NCT number | NCT05904418 |
Other study ID # | W1001 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 15, 2023 |
Est. completion date | June 9, 2023 |
Verified date | June 2023 |
Source | Balgrist University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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: - Is a 3D reconstruction of a lumbar spine from robot-assisted US scanning equivalent to or better quality than a 3D reconstruction from handheld US scanning? - Can a machine learning algorithm automatically segment the bone anatomy from robot-assisted and handheld US scanning to generate 3D lumbar spine reconstructions? - Can pedicle screw trajectories be identified based on posterior vertebral landmarks of 3D reconstructions of lumbar spines from both robot-assisted and handheld US scanning? Participants will: - fill out a medical history questionnaire - get clinically examined - have an ultra-low-dose (ULD) CT Scan of the vertebra L1 to S1 - have a handheld US scan of the vertebra L1 to S1 - have a robot-assisted US Scan of the vertebra L1 to S1 - fill out a post-study questionnaire
Status | Completed |
Enrollment | 63 |
Est. completion date | June 9, 2023 |
Est. primary completion date | June 9, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - Oral and written informed consent from the volunteer - Volunteers aged =18 y/o and =35 y/o - BMI above or equal to 19 kg/m2 or below or equal to 25 kg/m2 - Proficient in German or English language 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: - Chiropractic adjustment therapy - Injections such as local anesthetics and corticosteroids - Surgery - 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 |
Country | Name | City | State |
---|---|---|---|
Switzerland | University Hospital Balgrist, Balgrist Campus | Zurich |
Lead Sponsor | Collaborator |
---|---|
Philipp Fürnstahl | KU Leuven, Swiss Center for Musculoskeletal Imaging |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Target registration errors between US reconstructions and ground truth CT data | Evaluating the accuracy of the US reconstructions | Up to 1 year | |
Primary | Pedicle screw placement - Trajectory errors in terms of position | Evaluating the positional accuracy of the Pedicle screw placement | Up to 1 year | |
Primary | Pedicle screw placement - Trajectory errors in terms of direction | Evaluating the directional accuracy of the Pedicle screw placement | Up to 1 year | |
Secondary | Gender | female, male, non-binary, do not know, other | Up to 4 weeks | |
Secondary | Age | in years | Up to 4 weeks | |
Secondary | Smoking status | yes/no; if yes, pack years | Up to 4 weeks | |
Secondary | BMI | weight and height | Up to 4 weeks | |
Secondary | Tegner activity score | Subjective activity score of the volunteers | Up to 4 weeks | |
Secondary | ODI Oswestry Low Back Pain Disability Index | Standardized Low Back Pain Disability Index | Up to 4 weeks |
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