Agreement Between Artificial Intelligence and Anesthesiologists in Ultrasound-Guided Axillary Brachial Plexus Block

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorGaziantep City Hospital

About this trial

This prospective observational study aims to evaluate the agreement between artificial intelligence (AI)-assisted target point identification and experienced anesthesiologists during ultrasound-guided axillary brachial plexus block.

Ultrasound guidance is widely used in regional anesthesia to improve block success and safety. However, accurate identification of anatomical structures and optimal injection points remains operator-dependent. Artificial intelligence-based systems have the potential to assist clinicians by identifying anatomical landmarks in real time.

In this study, AI-generated target points will be compared with those determined by experienced anesthesiologists. The level of agreement between the two methods will be analyzed. Secondary outcomes will include block performance parameters and image quality.

The findings of this study may contribute to understanding the clinical utility of AI in ultrasound-guided regional anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 and 80 years

American Society of Anesthesiologists (ASA) physical status I-III

Patients scheduled for upper extremity surgery under ultrasound-guided axillary brachial plexus block as part of routine clinical practice

Ability to obtain adequate real-time ultrasound imaging of the axillary region prior to block performance

Disqualifiers

Inability to clearly visualize the axillary artery and at least one peripheral nerve (median, ulnar, radial, or musculocutaneous) on ultrasound imaging

Presence of significant ultrasound artifacts impairing image interpretation

History of previous surgery in the axillary region causing anatomical distortion

Anatomical deformities or significant anatomical variations in the axillary region

Trial population

Adult patients aged 18-80 years with American Society of Anesthesiologists (ASA) physical status I-III undergoing upper extremity surgery under ultrasound-guided axillary brachial plexus block in routine clinical practice. Only patients with adequate real-time ultrasound imaging of the axillary region allowing identification of relevant anatomical structures will be included.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Ultrasound-Guided Axillary Brachial Plexus Block (Routine Clinical Practice)

    Procedure/Surgery

    Ultrasound-guided axillary brachial plexus block performed as part of routine clinical care. No additional intervention is introduced for the purposes of the study. Real-time ultrasound images obtained during the procedure will be analyzed by an artificial intelligence system and experienced anesthesiologists.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Patients Undergoing Ultrasound-Guided Axillary Brachial Plexus Block1 intervention

Trial outcomes

Primary outcomes

1

Agreement in Target Point Identification Between Artificial Intelligence and Anesthesiologists

Agreement between artificial intelligence (AI) and experienced anesthesiologists in identifying target injection points will be evaluated using the intraclass correlation coefficient (ICC). Target points will be defined using coordinate-based measurements on real-time ultrasound images.

Time frame
During block procedure (ultrasound imaging)

Secondary outcomes

1

Proportion of Measurements Within Clinically Acceptable Agreement

The proportion of target point measurements with a difference of ≤5 mm between AI and anesthesiologists will be calculated. A difference of ≤5 mm will be considered clinically acceptable agreement.

Time frame
During block procedure
2

Agreement in Nerve Identification

Agreement between AI and anesthesiologists in identifying peripheral nerves (median, ulnar, radial, and musculocutaneous) will be evaluated using Cohen's kappa coefficient.

Time frame
During block procedure
3

Spatial Difference Between Target Points

The absolute distance (in millimeters) between AI-generated and anesthesiologist-defined target points will be calculated for each measurement.

Time frame
During block procedure

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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