CompletedNot Applicable

Clinical Validation of Nerveblox, an Artificial Intelligence Software to Support Ultrasound-Guided Regional Anesthesia Procedures

United States40 participantsStarted 2025-01-13

Plain-language summary

This single-center, prospective study is being conducted at AABP Integrative Pain Care and Wellness in Brooklyn, New York, USA. The aim of this study is to collect ultrasound images from healthy volunteers and evaluate the performance of the Nerveblox software using this image dataset. Nerveblox is a software as a medical device which is designed to assist anesthesiologist for ultrasound-guided regional anesthesia, prior to needling procedure.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * In good general health Exclusion Criteria: * Pregnancy * Inability to lie to flat * Any complaint or anatomical deformity on the regions to be scanned

What they're measuring

Performance assessment of anatomical landmark detection and highlighting of Nerveblox Software

Timeframe: Up to 35 days from enrollment

Trial details

NCT IDNCT06878911

SponsorSmart Alfa Teknoloji San. ve Tic. A.S.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-02-23

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