Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06550193

The Use of Augmented Reality (AR) or Virtual Reality (VR) to Enhance the Precision and Accuracy of Ultrasound-guided Medical Procedures

Led by Stanford University · Updated on 2026-05-07

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of augmented reality (AR) and virtual reality (VR) technology to improve ultrasound-guided medical procedures such as regional anesthesia and line placement. The study aims to determine whether AR/VR can enhance visualization of anatomical structures, improve the accuracy of needle placement, and reduce complications during these procedures. It also seeks to assess clinician usability and acceptance of these technologies to potentially improve patient outcomes and expand access to quality healthcare. Participants will undergo ultrasound-guided procedures using AR/VR devices designed to improve ergonomics and procedural precision. The study involves applying AR/VR technology during the procedure, while all participants receive standard pre- and post-procedure care. The study focuses on the feasibility and effectiveness of integrating AR/VR in clinical settings, with no comparison group mentioned. During the study, researchers will monitor procedure success rates, post-operative opioid use, and pain scores within 12 hours after surgery. They will also assess clinician satisfaction, procedure duration, needle passes or redirections, and needle visualization shortly after the procedure. Participants will be followed through these assessments to provide data on the potential benefits and challenges of AR/VR technology in medical procedures.

CONDITIONS

Brief Title

Augmented Reality/Virtual Reality (AR/VR) for Ultrasound-guided Medical Procedures

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients presenting for ultrasound-guided procedures
  • ASA physical status I, II, or III
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Incarceration
  • Body mass index (BMI) greater than 35

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Single procedure day

Participants undergo ultrasound-guided medical procedures using augmented reality (AR) or virtual reality (VR) technology.

1 procedure visit (in-person)

Post-procedure Monitoring

Duration - 12 to 24 hours after procedure

Participants are observed for post-procedure outcomes including pain scores, opioid consumption, and clinician satisfaction.

1 follow-up visit (in-person or remote)

Trial Site Locations

Total: 1 location

1

Stanford Hospital and Clinics

Stanford, California, United States, 94305

Actively Recruiting

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Research Team

J

Jean-Louis Horn, MD

K

Ksenia (kasimova), MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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