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Clinical Trial Summary

This is a single-centre, prospective, non-randomised volunteer study to be undertaken in the MediCentre, Heath Park, Cardiff, UK


Clinical Trial Description

This is a single-centre, non-randomised, prospective study involving at least 120 participants. The data collected in this study will augment the data collected in IU2019_AG_03 Volunteers will be enrolled sequentially until at least 120 scans have been recorded. Ideally, between 120 and 150 scans will be recorded. Phase I Data collected from up to the first 80 participants in each of the six peripheral nerve block areas will be used as a training/verification set. This set will be used to develop and verify models for the identification and highlighting of target anatomical structures on ultrasound images. Phase II The remaining 40 videos in each area (total minimum 120 participants) will be used for validation of these models. The validation videos will be fed into the models created during Phase I of the study and the output anatomy highlighting will be recorded as a separate video, overlaid on the original ultrasound image. The overlay video will then be further split into 30-second segments. A panel of three independent expert anaesthetists will be convened to review and score the segments for accuracy and performance to the endpoints agreed in Phase I of the study. ;


Study Design


Related Conditions & MeSH terms

  • Ultrasound Imaging of Anatomical Structures

NCT number NCT04277169
Study type Observational
Source IntelligentUltrasound Limited
Contact
Status Completed
Phase
Start date February 1, 2020
Completion date September 1, 2020

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