Clinical Trials Logo

Clinical Trial Summary

This is a single-center, prospective study to be undertaken at University of Oregon, Portland, USA. The aim is to evaluate the clinical performance of ScanNav Anatomy PNB when highlighting anatomical structures during UGRA scanning. Specifically, we aim to assess and quantify the correct/incorrect highlighting of anatomical structures associated with ScanNav Anatomy PNB during UGRA scanning.


Clinical Trial Description

Background: The American Society of Regional Anesthesia and Pain Medicine (ASRA) has published evidence-based assessment of ultrasound-guided regional anesthesia (Neal et al., 2010) concluding that ultrasound guidance is superior or equal to other non-ultrasound nerve localization techniques. A subsequent publication from ASRA (Neal et al., 2016), has strengthened their position of ultrasound guidance being superior than other methods, including for the reduction of local anesthetic systemic toxicity. However, ultrasound-guided regional anesthesia (UGRA) is a difficult technique to master. A key activity of UGRA is ultrasound image interpretation (Sites et al., 2009) which ScanNav Anatomy PNB is designed to support. The data collected during this study will be assessed by a panel of intended users (experts in UGRA) to evaluate the performance and safety of ScanNav Anatomy PNB device highlighting. Statistical Methodology: Validation analyses will be conducted once the data collection has been complete. The collected scans will be processed, and the device output will be generated post hoc. Device output will be presented with raw ultrasound side-by-side. A panel of at least three expert anesthesiologists will review and evaluate each processed scan. The majority view of the panel will be used to evaluate each endpoint for any given structure ScanNav Anatomy PNB is intended to highlight. Data collection and scan processing: 40 different subjects will be scanned. The dataset will be balanced to contain approximately equal numbers of subjects with BMI<30 and BMI>= 30 kg/m2. All data collection will be performed with FDA cleared general purpose ultrasound machine, ScanNav Anatomy PNB device will not be used during data collection. Data characteristics for scan subjects (e.g., age and BMI) will be reported. Ultrasound scans for all 9 supported anatomical regions will be collected from both sides of each subject. 90 x 10s clips per supported anatomical region will be generated, consisting of: - 80 x 10s scene clips: the block view (chosen by the expert scanner) together with the preceding 10 seconds of ultrasound scanning will be recorded (without the use of ScanNav Anatomy PNB) - 10 x 10s non-scene clips: 10 second ultrasound scans will be recorded at non-optimum block views, chosen by the expert scanner to represent plausible scanning errors (without the use of ScanNav Anatomy PNB) Scenes and non-scenes will be analyzed separately. Unmodified ultrasound video and highlighted video (color overlay produced by ScanNav Anatomy PNB generated post-hoc) will be presented side-by-side to independent experts for data analysis. Data analysis: Every clip will be presented to a minimum of 3 independent expert reviewers. All clips from a single anatomical region will be reviewed by the same 3 reviewers. Experts may review more than one anatomical region, but not necessarily all anatomical regions. Thus, a range of experts will review all anatomical regions. Reviewers will be asked structured questions to assess the highlighting of safety critical anatomical structures (see definitions later in document) and the performance of ScanNav Anatomy PNB output for each individual clip. The majority opinion (at least 2/3) will be obtained to establish the overall panel opinion (e.g., yes/yes/no = yes) for each structure on each clip. Data will be evaluated and presented by structure in each anatomical region and overall (i.e., total for each class; nerve, artery etc.). Inter-rater agreement between the reviewers will be reported on an anatomical region basis. Data will be presented as frequencies and presented as percent of total clips analyzed. Data analysis will include stratification by subject age, BMI, and ultrasound machine to ensure consistency across these variables. ;


Study Design


Related Conditions & MeSH terms

  • Ultrasound Imaging of Anatomical Structures

NCT number NCT04906018
Study type Observational
Source IntelligentUltrasound Limited
Contact
Status Completed
Phase
Start date May 16, 2021
Completion date November 30, 2021

See also
  Status Clinical Trial Phase
Completed NCT03654300 - A Volunteer Study to Collect Imaging Data for the Development of the Medaphor Anatomy Guide.
Active, not recruiting NCT04983771 - Validity of Experts and ScanNav Anatomy PNB When Identifying Sono-anatomical Structures for Ultrasound-Guided Regional Anaesthesia
Completed NCT05583032 - An Evaluation of the Long-Term Impact of Assistive AI on Anaesthetists' Ultrasound Scanning for UGRA
Completed NCT04918693 - A Study to Evaluate the Performance and Potential Benefits of an Assistive Artificial Intelligence Device ScanNav Anatomy Peripheral Nerve Block - US V1.0 for Ultrasound-guided Regional Anesthesia
Completed NCT04830891 - A Volunteer Study to Collect Imaging Data for the Development and Validation of ScanNav Anatomy PNB
Completed NCT04277169 - A Volunteer Study to Collect Imaging Data for the Development of the IntelligentUltrasound Anatomy Guide
Completed NCT05156099 - Clinical Performance Study: Evaluate Scanning & Interpretation Performance With & Without ScanNav Anatomy PNB
Completed NCT06375603 - Nerve and Plane Block Data Collection Study for the Development of Artificial Intelligence-assisted Software
Completed NCT04040179 - A Volunteer Study to Collect Imaging Data for the Development of the ntelligentUltrasound Anatomy Guide
Completed NCT06025279 - Musculoskeletal System Ultrasound Examination Data Collection Study for the Development of an Artificial Intelligence Software