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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04279808
Other study ID # 10-2019-3
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 2020
Est. completion date January 2021

Study information

Verified date February 2020
Source Seoul National University Hospital
Contact Jung-Man Lee, M.D.,PhD.
Phone +82-2-870-2513
Email jungman007@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

For safe central catheterization, clinicians must be aware of adequate dilator insertion depth not to directly dilate the venous wall. The purpose of the study is to find out adequate insertion depth of the dilator during central venous catheterization through the internal jugular vein with the aid of real-time ultrasonography.


Description:

This randomized controlled trial is to compare the distance between the skin puncture site and the outside of anterior wall of the internal jugular vein measured by real-time ultrasonography with the conventional method which is routinely used in common clinical practice.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 68
Est. completion date January 2021
Est. primary completion date January 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- adult patients requiring central venous catheterization through the right internal jugular vein

Exclusion Criteria:

- suspicion for infection of the right neck site

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
dilator depth
For soft tissue dilation just after guidewire insertion in central venous catheterization through the right internal jugular vein, investigators will measure the distance between the skin puncture site and outside of anterior wall of the vein with real-time ultrasonography in the measured depth group. Next, practitioner will insert the dilator by the measured length and continue to insert the central venous catheter. For the conventional group as a control group, practitioner will perform the central venous catheterization with a manner used routinely by the practitioner.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital SMG-SNU Boramae Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary hematoma realted with the dilator hematoma from the vascular wall puncture by the dilator 1 Day (on the study day for each patient)
Secondary distance between skin puncture site and the outside of the anterior wall of the internal jugular vein distance between skin puncture site and the outside of the anterior wall of the internal jugular vein which will be measured by real-time ultrasonography 1 Day (on the study day for each patient)
See also
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