Novel Device for Ultrasound-guided Pediatric Vessel Cannulations

NCT04039490 · tracked via the Priya Life Science USA tracker

Sponsor

Clear Guide Medical

Phase

Not applicable

Started

2024-02-06

Last updated

2024-09-26

Condition(s) studied

Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients

Investigational drug(s) / intervention(s)

SCENERGY

SCENERGY: Use of the SCENERGY guidance device in conjunction with ultrasound to guide needles for pediatric vessel cannulations

Study summary

Clinical Trial to investigate whether the use of a novel device to be used in conjunction with ultrasound in pediatric vessel cannulations is superior to ultrasound-only pediatric vessel cannulations in terms of number of cannulation attempts.

Eligibility

Sex

ALL

Min age

1 Month

Max age

17 Years

Healthy volunteers

Inclusion Criteria: * any pediatric patient scheduled for a vessel cannulation at CNMC Exclusion Criteria: * none

Primary outcome measure(s)

Successful first-attempt vessel cannulation — 1 hour
Test if the vessel cannulation was successful with only 1 attempt --needle puncture--to reach the vessel

Trial sites (1)

Facility	City	Region	Status
Children's National Medical Center	Washington D.C.	District of Columbia	Recruiting

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04039490 on ClinicalTrials.gov ↗ ← All trials in the USA