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Ultrasound Imaging of Anatomical StructuresNCT04983771

Validity of Experts and ScanNav Anatomy PNB When Identifying Sono-anatomical Structures for Ultrasound-Guided Regional Anaesthesia

An observational study of Ultrasound Imaging of Anatomical Structures, run by IntelligentUltrasound Limited at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This is a multi-centre, prospective, observational study, conducted under the auspices of the University of Oxford to evaluate ultrasound image analysis by human experts and an artificial intelligence device in the context of ultrasound-guided regional anaesthesia (UGRA). Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
What is being tested?
Annotate ultrasound scans
Type of treatment
Medical device
How many people
19 participants
Where
1 siteUnited Kingdom
Study dates
1 Sep 2021to 6 May 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: At least 15 UGRA experts will be recruited from seven centres in the UK.

Who may be able to join

  • Member of a relevant professional society (e.g., RA-UK, ESRA, ASRA) and meets at least three of the following criteria:
  • Completed advanced training in UGRA or have >10 years of independent practice in UGRA
  • Hold a qualification related to UGRA (e.g., EDRA, higher degree or equivalent)
  • Regularly delivers direct clinical care using UGRA, including for 'awake' surgery where indicated
  • Regularly teaches UGRA in the course of their clinical work, including advanced techniques (Plan B/C/D blocks) where indicated

Who cannot join

  • none

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Intelligent Ultrasound Limited

    Cardiff, Wales, CF10 1DY

Other trials in United Kingdom

About this study

Official title: Anatomical Validity of Experts and ScanNav Anatomy PNB When Identifying Sono-anatomical Structures for Ultrasound-Guided Regional Anaesthesia

This is a multi-centre, prospective, observational study, conducted under the auspices of the University of Oxford to evaluate ultrasound image analysis by human experts and an artificial intelligence device in the context of ultrasound-guided regional anaesthesia (UGRA).

Read the detailed description

Ethical Approval:

The ultrasound scans/still frame images used in this study have been acquired from an earlier study conducted at Oregon Health \& Science University (OHSU) (ClinicalTrials.gov ref: NCT04906018). OHSU Institutional Review Board approval (STUDY00022920) was granted for collection of the ultrasound scans.

Ethical approval for the assessment of these scans by regional anaesthesia experts, has been obtained from Oxford University Research Ethics Committee for Medical Sciences (R75449/RE001).

Block Areas Included:

A Delphi study was undertaken earlier in the research programme: 'International Consensus on the Minimum Anatomical Structures to Identify on Ultrasound for the Performance of Plan A Blocks in Ultrasound-Guided Regional Anaesthesia: A Regional Anaesthesia UK Delphi Study' (work currently unpublished).

As ScanNav Anatomy PNB has undergone development and validation work for all of these blocks apart from the femoral nerve block, the remaining six Plan A block regions will be considered for this project. These regions (and structures assessed) are:

  • Interscalene level brachial plexus (Structures: anterior scalene, middle scalene, C5 nerve root, C6 nerve root)
  • Axillary level brachial plexus (Structures: axillary artery, axillary vein, conjoint tendon, median nerve, musculocutaneous nerve, radial nerve, ulnar nerve)
  • Erector spinae plane (Structures: transverse process, erector spinae muscle group)
  • Rectus sheath plane (Structures: rectus abdominis, rectus sheath (anterior layer), rectus sheath (posterior layer), peritoneum)
  • Adductor canal (Structures: femoral artery, sartorius, saphenous nerve/nerve complex)
  • Popliteal level sciatic nerve (Structures: sciatic nerve)

Standardisation of Ultrasound Scans used for Assessment:

The ultrasound videos and still frames will undergo review during the earlier (OHSU) study, including the following:

  1. Does this ultrasound scan obtain the correct view for this block? [Yes/no]
  2. Does the video or still frame contain any atypical anatomy? [Yes/no]

The answer for question 1 must be 'Yes' and for question 2 must be 'No' for the scan to be included in the present study.

Selecting Ultrasound Scans for Assessment:

Of the acceptable ultrasound scans, five will be selected (at random) for each region. This will be done for each of the six block regions, providing a total of 30 scans/still frame images overall. A suitable still frame in each scan sequence will be selected by the investigators and saved as an image file in the Portable Network Graphic (PNG) format for later segmentation.

Expert Reviewers:

Approximately 15 UGRA experts will be recruited from centres in the UK. One-three will be recruited from each of seven centres:

  • Aneurin Bevan University Health Board
  • Guy's \& St Thomas' NHS Foundation Trust
  • NHS Greater Glasgow \& Clyde
  • NHS Tayside
  • Oxford University Hospitals NHS Foundation Trust
  • Imperial College Healthcare NHS Trust
  • Royal Cornwall Hospitals NHS Trust

All experts must hold a UK-recognised qualification for independent practice in anaesthesia (i.e., be qualified to perform UGRA independently and supervise others) and be a member of a relevant professional society (e.g., RA-UK, ESRA, ASRA). They must also meet at least three elements of the following criteria:

  • Completed advanced training in UGRA or have >10 years of independent practice in UGRA
  • Hold a qualification related to UGRA (e.g., EDRA, higher degree or equivalent)
  • Regularly delivers direct clinical care using UGRA, including for 'awake' surgery where indicated
  • Regularly teaches UGRA in the course of their clinical work, including advanced techniques (Plan B/C/D blocks) where indicated

Defining the Ground Truth:

The UGRA experts will all view each video in turn, on a tablet computer. At the end of each one they will be asked to mark the boundaries of the relevant anatomical structures (listed above) for the corresponding still frame image using the tablet and a stylus.

There are 21 anatomical structures across all the regions assess. Each region will represented by five ultrasound scans. Thus, 105 structures (21 x 5) will each be assessed by around 15 experts. The expert segmentation masks (for each annotated structure) will be processed in the following manner to derive an average mask for each structure:

  • Each segmentation mask, ms, for a given structure will be segmented such that ms = f(m) = {1 if mask present 0 if mask not present
  • For each pixel, ps, the frames will be summed across all n segmentation masks
  • This will give a final mask, mf, where mf = { p : 0 ≤ p ≤ n }
  • The mf will then be filtered with a threshold such that mt = f2(mt) = { 1 if pf > t n 0 otherwise

In the above description, ms represents a segmentation mask produced by each expert. Areas enclosed by an expert's segmentation outline will be allocated a numerical value of 1 (0 if not enclosed by an area of segmentation). Each pixel in the final mask (mf) will be summed across all (n) the segmentation masks of the experts, to give a final value of 0 - n. At least 75% of experts must enclose the pixel in their individual segmentation mask for the pixel to be included in the overall ground truth. ≥75% has been chosen to be consistent with the strong recommendations made in the earlier Delphi study. Lastly, mf will then be filtered at this threshold to produce the ground truth mask (mt). The algorithm defined above will be run using Python2 in jupyter-lab ('Project Jupyter').

Variability in Expert Analysis:

The correlation in the expert markings will be compared using the Dice/Intersection over Union (IoU) and Hausdorff co-efficients. Dice/IoU will be used for all structures except those identified by a non-enclosed area, where the Hausdorff co-efficient will be used. These structures are:

  • Conjoint tendon
  • Transverse process
  • Rectus sheath (anterior layer)
  • Rectus sheath (posterior layer)
  • Peritoneum

Comparison to ScanNav Anatomy PNB:

The ground truth will provide an expert 'gold standard' against which ScanNav Anatomy PNB will be compared. The level of correlation of ScanNav Anatomy PNB highlighting will be compared to the expert ground truth in the same statistical manner as above

Being tested
Annotate ultrasound scans

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Annotate ultrasound scansDevice

    Each expert will be asked to hand-labelled anatomical structures on relevant ultrasound images

Study groups in NCT04983771
Study groupRoleWhat they receive
Expert in ultrasound-guided regional anaesthesiaAt least 15 UGRA experts, member of a relevant professional society (e.g., RA-UK, ESRA, ASRA) and meeting at least 3 of the following criteria) will be recruited from centres in the UK. * Completed advanced training in UGRA or have >10 years of independent practice in UGRA * Hold a qualification related to UGRA (e.g., EDRA, higher degree or equivalent) * Regularly delivers direct clinical care using UGRA, including for 'awake' surgery where indicated * Regularly teaches UGRA in the course of their clinical work, including advanced techniques (Plan B/C/D blocks) where indicated
Receives: Device: Annotate ultrasound scans

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Experts' variability

    Assess variability in identification of key anatomical structures on ultrasound by individual members of the expert panel

    Measured: 2 years

  2. ScanNav anatomy PNB comparison

    Compare the identification of anatomical structures on ultrasound images by an artificial intelligence system to the combined assessment of a panel of experts

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jul 2021
  2. Study start1 Sep 2021
  3. Primary completion6 May 2022
  4. Study completion6 May 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
19 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04983771
Sponsor's protocol ID
R75449/RE001-1
Status last verified
Aug 2023
First submitted
21 Jul 2021
Last updated
1 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Ultrasound Imaging of Anatomical Structures, run by IntelligentUltrasound Limited at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Experts' variability (time frame: 2 years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2024.

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