Ultrasound Guided Axillary Venous Cannulation in Pediatrics

Seoul National University

Status: Completed

Conditions: Ultrasound Guided Central Venous Cannulation

Treatments: Device: landmark; Device: US_Ax

Study type: Interventional

Funder types: Other

Identifiers

NCT02806401

H-1603-111-750

Details and patient eligibility

About

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.

Full description

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).

Enrollment: 132 patients

Sex: All

Ages: 1 month to 7 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• surgery under general anesthesia require central venous catheterization

Exclusion criteria

• hematoma in central vein central vein anomaly catheterization site infection

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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132 participants in 2 patient groups

landmark

Experimental group

Description:

landmark method_subclavian venous cannulation

Treatment:

Device: landmark

US_Ax

Active Comparator group

Description:

ultrasound guided axillary venous cannulation

Treatment:

Device: US_Ax