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Ultrasound Guided Axillary Venous Cannulation in Pediatrics

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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

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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