Handheld US Device to Verify Vascular Cannulation
NCT: NCT07722065 · ENROLLING_BY_INVITATION
Brief 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).
Frequently Asked Questions
What is Handheld US Device to Verify Vascular Cannulation?
Handheld US Device to Verify Vascular Cannulation is a clinical trial registered under NCT07722065. Current status: ENROLLING_BY_INVITATION.
What is the status of NCT07722065?
The current status of NCT07722065 (Handheld US Device to Verify Vascular Cannulation) is: ENROLLING_BY_INVITATION.
When did Handheld US Device to Verify Vascular Cannulation start?
Handheld US Device to Verify Vascular Cannulation started on 2026-08.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.