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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02312388
Other study ID # H-1303-113-478
Secondary ID
Status Completed
Phase N/A
First received November 27, 2014
Last updated December 8, 2014
Start date July 2013
Est. completion date May 2014

Study information

Verified date December 2014
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the differences in central venous catheter insertion time, success rate, and complication between thin-wall needle technique and catheter-over-the-needle technique for central venous catheterization in children.


Description:

Catheterization was performed using ultrasound with an "out-of-plane" approach by inserting the introducer needle (thin-wall needle technique) or Angiocath Plus™ catheter (catheter-over-the-needle technique) in 45 - 60° to the patient's skin while viewing the vein in a cross section.


Recruitment information / eligibility

Status Completed
Enrollment 138
Est. completion date May 2014
Est. primary completion date February 2014
Accepts healthy volunteers No
Gender Both
Age group N/A to 5 Years
Eligibility Inclusion Criteria:

- surgery under general anesthesia

- require central venous catheterization

Exclusion Criteria:

- hematoma in central vein

- central vein anomaly

- catheterization site infection

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
catheter-over-the-needle technique
using a 22 G Angiocath Plus™ catheter
Thin-wall needle technique
using 18 - 21 G introducer needle

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Guide-wire insertion time interval between skin penetration and removal of the needle or catheter after guide wire insertion, an expected average of 80 seconds No
Secondary Time to first puncture of central vein interval between skin penetration of the needle or catheter and flashback of blood, an expected average of 25 seconds No
Secondary Total time of central venous catheter insertion interval between skin penetration of the needle or catheter and installation of the indwelling catheter, an expected average of 3 minutes No
Secondary Number of central vein puncture trial up to 5 times, an expected average observation time of 25 seconds No
Secondary Number of guide-wire insertion trial up to 5 times, an expected average observation time of 80 seconds No
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