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Clinical application of Mixed Reality and Head-mounted Display in intermuscular groove brachial plexus block.

Clinical application of Mixed Reality and Head-mounted Display in intermuscular groove brachial plexus block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091595
Enrollment
Unknown
Registered
2024-10-30
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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:The operators in the control group will perform the procedure by visualizing the conventional ultrasound images displayed directly on the ultrasound screen. Each operator will perform in
Experimental: MR+HMD group:In the MR + HMD group, the ultrasound machine will be located behind the operator to remove the distraction, and the operator will not be allowed to see the ultrasound scree

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: Wireless mixed reality ultrasound glasses for interscalene brachial plexus block application: Patients: Age = 18 years, patients who voluntarily undergo ultrasound-guided interscalene brachial plexus block, and sign an informed consent form Doctor: Attending anesthesiologist with 5 years of experience in nerve block;

Exclusion criteria

Exclusion criteria: Patient: declined to participate in the study; The puncture site has infection, abnormal coagulation function, abnormal mental incompatibility or nerve injury. Serious heart, respiratory, kidney or liver disease; Abnormal coagulation function; Chronic pain disease existed before operation; Using analgesics or receiving psychotropic medication; Allergic to local anesthetics or ultrasonic coupling agents; Doctor: Less than 5 years of experience in nerve block.

Design outcomes

Primary

MeasureTime frame
Total duration of nerve block ;

Secondary

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

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