A novel electromagnatic ultrasound-guided central vein cannulation comparing with conventional ultrasound-guided technique in pediatric patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009941

Enrollment

Registered

2024-11-22

Start date

2022-08-02

Completion date

Unknown

Last updated

2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : This study was performed on 90 patients who underwent prospective randomization and underwent central venous catheter insertion during surgery. If it is decided to participate in this

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Pediatric patients under the age of 4 who need central venous catheter insertion during surgery - Weight less than 20kg

Exclusion criteria

Exclusion criteria: - Vascular malformations - hemodynamically unstable child - Previous history of central venous catheter insertion with femoral vein - emergency surgery

Design outcomes

Primary

Measure	Time frame
primary endpoint: success rate on first attempt (success / fail)	—

Secondary

Measure	Time frame
secondary endpoint: complication rate (arterial puncture, vascular wall puncture, rate of hematoma incidence);Finally, the success rate, the number of punctures (n), the success rate of blood aspiration;Time to puncture success (T1, sec);Time (T2, sec) from successful aspiration of the blood until the central vein was stabilized	—

Countries

Korea, Republic of

Contacts

Public Contacthyojin byon

Yonsei University

jinoben@naver.com+82-2-2228-2429

Outcome results