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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04277169
Other study ID # IU2020_AG_04
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date September 1, 2020

Study information

Verified date February 2021
Source IntelligentUltrasound Limited
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date September 1, 2020
Est. primary completion date May 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Male or female, at least 18 years of age; 2. Able to comprehend and sign the Informed Consent prior to enrolment in the study. Exclusion Criteria: 1. Aged <18 years of age; 2. Unwilling or unable to provide informed consent.

Study Design


Related Conditions & MeSH terms

  • Ultrasound Imaging of Anatomical Structures

Locations

Country Name City State
United Kingdom MediCentre, Heath Park Cardiff Wales

Sponsors (1)

Lead Sponsor Collaborator
IntelligentUltrasound Limited

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Model development and verification Collection of ultrasound scans. The collected scans will be assessed and used in the development and verification of deep-learning models that identify the target structures using a training dataset. 4 months
Secondary Model validation Estimation of performance and accuracy (e.g. success/failure of highlighting of target structures, average distance of highlighting from target, time spent highlighting correct structure as a proportion of time target visible) 4 months
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