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Clinical Trials/NCT05399875
NCT05399875
Active, not recruiting
Not Applicable

Augmented Reality Ruler to Improve Safety and Clinical Workflow During Placement of Peripherally Inserted Central Catheters

University of Pennsylvania1 site in 1 country20 target enrollmentSeptember 26, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Insertion of Peripherally Inserted Central Catheter
Sponsor
University of Pennsylvania
Enrollment
20
Locations
1
Primary Endpoint
Number of participants with appropriate catheter tip location
Status
Active, not recruiting
Last Updated
7 months ago

Overview

Brief Summary

The purpose of this study is to assess the utility of an augmented reality virtual ruler during placement of peripherally inserted central catheters.

Detailed Description

After being informed about the study, patients who give consent will have their peripheral inserted central catheter placed by a physician wearing mixed reality smart glasses. The mixed reality smart glasses will have an application that allows the physician to measure distances with their hands. This application will be used to measure the appropriate length for which to trim the central catheter.

Registry
clinicaltrials.gov
Start Date
September 26, 2022
End Date
June 30, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ali Dhanaliwala

Physician

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • Scheduled for a non-emergent peripherally inserted central catheter placement in Interventional Radiology
  • Over 18 years

Exclusion Criteria

  • Undergoing an emergent peripherally inserted central catheter placement
  • Younger than 18 years old

Outcomes

Primary Outcomes

Number of participants with appropriate catheter tip location

Time Frame: End of procedure

Catheter tip location will be evaluated by the treating physician on x-ray

Secondary Outcomes

  • Procedure time(End of procedure)
  • Radiation dose(End of procedure)

Study Sites (1)

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