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NCT05710445 Clinical Trial

Augmented Reality Heads-up Display to Improve Ultrasound Guided IV Access

Phlebotomy Clinical Trial

Official title:
Augmented Reality Heads-up Display to Improve Ultrasound Guided IV Access

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT05710445
Other study ID # 852551
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date February 16, 2023
Est. completion date March 1, 2024

Study information
Verified date March 2024
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the utility of an augmented reality headset for visualization of ultrasound images during ultrasound guided placement of an intravenous catheter.

Description:

After being informed about the study, patients who require image guided intravenous access and give consent will have their intravenous catheter placed by a physician wearing mixed reality smart glasses. The mixed reality smart glasses will have an application that allows the physician to view the ultrasound images in a virtual monitor. The physician will then use the images viewed on this virtual monitor to guide placement of the intravenous catheter.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date March 1, 2024
Est. primary completion date March 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age =18 years - Referral for US assisted placement Exclusion Criteria: - Urgent/emergent requirement for IV

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Augmented Reality
Mixed reality smart glasses will be used to view a virtual monitor which mirrors the ultrasound screen in real-time.

Locations
Country Name City State
United States University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cannulation rate Number of successful venous cannulations as evaluated by treating physician At end of procedure, on average 30 minutes
Secondary Cannulation attempts Number of attempts needed to achieve a successful procedure At end of procedure, on average 30 minutes
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