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Novel Device for Ultrasound-guided Pediatric Vessel Cannulations

NCT04039490 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-09-26

No results posted yet for this 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.

Conditions

  • Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients

Interventions

DEVICE

SCENERGY

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

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH

  • Children's National Research Institute

    collaborator OTHER

  • Clear Guide Medical

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Month
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-06
Primary Completion
2025-08-31
Completion
2025-08-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04039490 on ClinicalTrials.gov