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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02878174
Other study ID # IJV_rotation
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 1, 2024
Est. completion date July 1, 2026

Study information

Verified date November 2023
Source Seoul National University Hospital
Contact Chul-Woo Jung Jung, MD
Phone 2-2-2072-0640
Email jungcwoo@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Two approaches such as ultrasound (US)-guided and prelocation techniques are possible when the internal jugular vein cannulation is attempted with US. This study is a clinical trial that compares the success rates of both techniques and shows the non-inferiority of the prelocation technique. However, during prelocation technique, rotated screen of the US is used instead of original screen. The angle of rotation is determined by the degree of rotation of US probe where an accelerometer is attached.


Description:

The investigator's own developed screen-rotating program is used. An accelerometer is attached on the front surface of the ultrasound (US) probe. The angle of rotation of the probe is delivered to the laptop and becomes the information to adjust the rotating angle of screen. Immediately after induction of general anesthesia, the patient's head is turned slightly, and the table is tilted at 10 degrees. In the US group, the investigators obtain a sonographic view and try a cannulation of the internal jugular vein (IJV). In the prelocation group, a skin marker is made on the anticipated skin puncture site where a perpendicular line that passes over the center of the IJV meets the skin on the rotated US screen. It is recorded "success" when the internal jugular vein is successfully punctured without complications. It is recorded "failure" if the internal jugular vein is not punctured during repeated needle passes. The number of tries and tile to success are recorded. The success and complication rates between two groups are compared.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 320
Est. completion date July 1, 2026
Est. primary completion date July 1, 2026
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - Patients scheduled for general anesthesia Exclusion Criteria: - Refusal of consent - Patients with cervical spine injuries - Patients with atlanto-axial instability - Patients at risk of increased intracranial pressure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
internal jugular vein catheterization
internal jugular vein catheterization using ultrasound (US) or US-based prelocation techniques

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate of internal jugular vein cannulation intraoperative
Secondary Degree of rotation of ultrasound (US) probe intraoperative
See also
  Status Clinical Trial Phase
Not yet recruiting NCT02492932 - The Second Try During Landmark Approach of the Internal Jugular Vein: an Ultrasonographic Prelocation Study N/A
Active, not recruiting NCT03030898 - Analysis of Respiratory Variations of the Right Internal Jugular Vein as a Predictor of Fluid Responsiveness During Mechanical Ventilation N/A
Completed NCT04761237 - The Value of Central Venous-arterial Carbon Dioxide Difference N/A