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Active Not Recruiting
NCT07722065
Handheld US Device to Verify Vascular Cannulation
Conditions: Surgery
Sex: All
Ages: 1 Year – 6 Years
Healthy volunteers: No
Phase: NA
Enrollment: 50
Sponsor: Alok Moharir
Location: Nationwide Children's Hospital Columbus Ohio
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).
Eligibility Criteria
Inclusion Criteria:
* pediatric patients ranging in age from 1-6 years
* presenting for surgery and requiring placement of an intravenous cannula.
Exclusion Criteria:
* potential subjects that are fluid or sodium sensitive
Source: ClinicalTrials.gov (NCT07722065). StuddyBuddy aggregates publicly available trial information.