Handheld US Device to Verify Vascular Cannulation

StatusActive, Not Recruiting
PhaseNot applicable
Started

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Record History

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  1. Minor Trial status changed: Enrolling by Invitation → Active, Not Recruiting Show 4 more changesShow less
    • Final enrollment: 50 participants (planned 100)
    • Start date changed from estimate of Aug 2026 to Sep 22, 2021
    • Site details revised
    • Eligibility criteria expanded, about 3 words
  2. Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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).
Trial Details
NCT Number NCT07722065
Lead Sponsor Alok Moharir
Conditions
(from sponsor)
Surgery
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov