CompletedNot Applicable

Clinical Performance Study: Evaluate Scanning & Interpretation Performance With & Without ScanNav Anatomy PNB

United Kingdom21 participantsStarted 2021-12-06

Plain-language summary

This is a single-centre, randomised, interventional prospective cohort study to be undertaken at offices of Intelligent Ultrasound Limited in Cardiff, United Kingdom.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Male or female, at least 18 years of age
✓. Able to comprehend and sign the Informed Consent prior to enrolment in the study
✓. Available to travel and attend the study day in person in Cardiff, UK
✓. Medical professional (currently practicing anaesthetist or similar clinician) who is qualified to perform UGRA
✓. Do not self-identify as an expert in the field of UGRA:
✓. Has not completed advanced training or hold a qualification (e.g., EDRA, MSc, MD, PhD) related to UGRA
✓. Does not regularly deliver anaesthesia for 'awake' surgery (excluding central neuraxial techniques)
✓. Does not teach on formal RA courses

Exclusion criteria

✕. Aged \<18 years of age
✕. Unwilling or unable to provide informed consent
✕. Expert in UGRA (see definition above)

What they're measuring

Correct identification of appropriate block site (at initial assessment and 2 months later)

Timeframe: 12 months

Trial details

NCT IDNCT05156099

SponsorIntelligentUltrasound Limited

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2022-12-08

View on ClinicalTrials.gov More Ultrasound Imaging of Anatomical Structures trials