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Completed

NCT Number: NCT02806401

Ultrasound Guided Axillary Venous Cannulation in Pediatrics

The purpose of this prospective randomized study was to compare landmark-subclavian venous access to ultrasound-guided axillary venous access when performed by pediatric anesthesiologists.

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Key information

Conditions

Ultrasound Guided Central Venous Cannulation

Age range

1 month–7 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jin-Tae Kim

Seoul, South Korea

About this study

Objective: Subclavian vein catheterization may cause various complications. The investigators will compare the real-time ultrasound-guided axillary venous access vs. the landmark method- subclavian venous access in pediatric paticipants. (the needle insertion point of ultrasound-guided axillary venous is axillary vein. and the needle insertion point of landmark method is infraclavicular subclavian vein)

Design: Prospective randomized study.

Setting: Operating room of a tertiary medical center.

Interventions: The investigators will compare the ultrasound-guided axillary vein cannulation (66 paticipants) vs. the landmark method (66 pa- ticipants).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • surgery under general anesthesia require central venous catheterization

Exclusion criteria

  • hematoma in central vein central vein anomaly catheterization site infection

Treatment and study plan

landmark

Device

US_Ax

Device

Primary outcomes

  1. 2nd access success rate

    Time frame: interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds

Secondary outcomes

  1. 1st access success rate

    Time frame: interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds

  2. 3rd access success rate

    Time frame: interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds

  3. total time

    Time frame: interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Official study title

Real-time Ultrasound-guided Axillary Venous Catheterization in Pediatric Patients: Comparison With the Landmark Technique Subclavian Vein Catheterization

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jun 20, 2016
Registry last updated
Sep 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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