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Clinical Trial

Handheld US Device to Verify Vascular Cannulation

NCT: NCT07722065 · ACTIVE_NOT_RECRUITING

NCT IDNCT07722065
StatusACTIVE_NOT_RECRUITING
Start Date2021-09-22
SponsorAlok Moharir (OTHER)
First posted
Last updated

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).

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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