Novel Device for Ultrasound-guided Pediatric Vessel Cannulations

Last updated: September 25, 2024
Sponsor: Clear Guide Medical
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

SCENERGY

Clinical Study ID

NCT04039490
CNMC Ph II Trial
  • Ages 1-17
  • All Genders

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 Criteria

Inclusion

Inclusion Criteria:

  • any pediatric patient scheduled for a vessel cannulation at CNMC

Exclusion

Exclusion Criteria:

  • none

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: SCENERGY
Phase:
Study Start date:
February 06, 2024
Estimated Completion Date:
August 31, 2025

Study Description

Use of needle guidance plus ultrasound imaging for CVC placement in the pediatric high-risk population may facilitate the procedure with a single needle pass and decrease the incidence of adverse effects by minimizing additional needle passes. This study will compare the use of ultrasound-only guidance with the Clear Guide SCENERGY guidance in terms of successful first-attempt vessel cannulations such as internal jugular and fermoral artery access. The question is whether it is possible to make ultrasound-guided pediatric vascular access less technically challenging in order to improve adoption and utilization leading to decreased iatrogenic complications and improved patient safety.

Connect with a study center

  • Children's National Medical Center

    Washington, District of Columbia 20910
    United States

    Active - Recruiting

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