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Application Effect of Smart Glasses-Assisted Ultrasound-Guided Venipuncture in Obese Patients by Junior Nurses

Application Effect of Smart Glasses-Assisted Ultrasound-Guided Venipuncture in Obese Patients by Junior Nurses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109050
Enrollment
Unknown
Registered
2025-09-10
Start date
2025-09-11
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Obesity

Interventions

Experimental group:1. The operator wears smart glasses (AR head-mounted display), which are connected to a portable ultrasound device via wireless technology, projecting real-time ultrasound images in
2. The operator performs venous identification and localization by observing the images in the smart glasses, completing peripheral venous puncture and catheter placement under visual guidance
3. This process can reduce the operator's frequent head-down movements to check the ultrasound screen during the operation, improving the coherence and efficiency of the procedure
4. During the intervention, the time spent by the operator observing images, the time spent observing the patient, the number of punctures, and the total time taken are recorded.
Control Group:1. The operator uses the same model of portable wireless ultrasound equipment, but the images are displayed on a conventional external display screen
2. The operator needs to frequently switch their gaze between the operating area and the display screen to complete peripheral venous puncture under ultrasound guidance
3. The puncture process and recorded indicators in this group are consistent with the experimental group to ensure that the intervention method is the only variable.

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. Age >= 18 years old; 2. BMI > 30 kg/m^2 (Obesity); 3. ASA classification II~III; 4. Scheduled for elective surgery under general anesthesia, requiring peripheral intravenous puncture; 5. The subject voluntarily participates in the study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who refuse to participate in this study; 2. Individuals with clotting function abnormalities; 3. Those with mental disorders who cannot cooperate; 4. Individuals allergic to ultrasound coupling agents.

Design outcomes

Primary

MeasureTime frame
First-attempt success rate of peripheral venous cannulation;

Secondary

MeasureTime frame
Time to first-attempt success (seconds):;

Countries

China

Contacts

Public ContactChen Hong

The Second Affiliated Hospital of Anhui Medical University

liuchengxiang2023@gmail.com+86 138 6670 5366

Outcome results

None listed

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