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ENROLLING BY INVITATION
NCT07722065
NA

Handheld US Device to Verify Vascular Cannulation

Sponsor: Alok Moharir

View on ClinicalTrials.gov

Summary

This a prospective study in pediatric patients undergoing surgery and requiring placement of an intravenous cannula. This will be a novel study to assess whether a handheld compatible cardiac ultrasound device (Lumify) can be used to quickly and reliably verify successful vascular cannulation in pediatric patients using the rapid atrial swirl sign (RASS) technique. As emerging technologies have made hand-held ultrasound devices more versatile, portable, and cheaper, it will be important to prove if they can be as accurate as traditional ultrasound devices for their intended focused point-of-care functions. If the handheld device is deemed efficacious, it will allow the use of a portable hand-held device rather than the more difficult to transport devices (Sonosite).

Official title: The Use of a Handheld Cardiac Ultrasound Device to Verify Successful Peripheral Vascular Cannulation in Pediatric Patients.

Key Details

Gender

All

Age Range

1 Year - 6 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-08

Completion Date

2027-12

Last Updated

2026-07-23

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Sonosite

A stand alone ultrasound machine with a linear probe.

DEVICE

Lumify®

A novel, handheld ultrasound device with a cardiac phase array probe attached to a tablet.

Locations (1)

Nationwide Children's Hospital

Columbus, Ohio, United States