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Clinical Application of Smart Glasses in Interscalene Brachial Plexus Block Performed by Junior Anesthesiologists

Clinical Application of Smart Glasses in Interscalene Brachial Plexus Block Performed by Junior Anesthesiologists

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117071
Enrollment
Unknown
Registered
2026-01-19
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Not involved

Interventions

Control group:Perform the operation using traditonal ultrasound
Experimental: smart glasses group:Perform the operation using smart glasses connected ultrasound

Sponsors

the Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient: Individuals aged =18 years who voluntarily consent to undergo ultrasound-guided intermuscular groove brachial plexus nerve block and have signed an informed consent form; 2. Physician: Trainee doctors who have completed training in ultrasound-guided intermuscular groove brachial plexus nerve block, have successfully performed the procedure, and have been certified by a senior consultant as possessing competent operational skills. 3. Physician: Senior anaesthetist with five or more years' experience in nerve block procedures.

Exclusion criteria

Exclusion criteria: 1. Patient: Refusal to participate in this study 2. Patient: Infection at puncture site, coagulation disorders, psychiatric conditions precluding cooperation, or nerve injury 3. Patient: Severe cardiac, respiratory, renal, or hepatic disease 4. Patient: Pre-existing chronic painful condition 5. Patient: Use of analgesic medications or psychiatric drug therapy 6. Patient: Allergy to local anaesthetics or ultrasound coupling agents; 7. Physician: Lack of training in ultrasound-guided interscalene brachial plexus block and absence of senior physician certification confirming competent execution capability

Design outcomes

Primary

MeasureTime frame
Total duration of nerve block;

Secondary

MeasureTime frame
Time from the probe to the skin breaking (T1);Time from the puncture needle breaking the skin to entering the target area (T2) ;Duration of the needle tip visible on the ultrasound image (T3);Total number of needle redirections;Ultrasound scan time;Sensory and motor block scores after 30 minutes of block;Satisfaction score of operators;Operator's head movement;The adequacy of drug infiltration around the target nerve was recorded;The incidence and severity of complications;Patient's pain scale score during the interscalene brachial plexus block;Satisfaction score of Patien;

Countries

China

Contacts

Public ContactLingling Jiang

the Second Affiliated Hospital of Anhui Medical University

lamar_00@126.com+86 138 6611 1607

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026