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Completed

NCT Number: NCT05656937

Oblique Versus Transverse Orientation Approach for Internal Jugular Venous Cannulation in Pediatrics

this study aimed to compare oblique versus transverse orientation approach in jugular venous cannulation in term of cannulation success in pediatric heart surgery patients

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Key information

About this study

Sixty patients randomised into two groups, 30 patients in experimental group (oblique orientation) and 30 patients in control group (transverse orientation). All cannulation took place in the operation room. Patients underwent general anesthesia and placed in supine position. Standard monitoring (electrocardiogram, non-invasive arterial pressure, pulseoxymetry) was carried out during the procedure for all patients. Before preparation of the skin, a pre-procedure ultrasound examination was performed to verify internal jugular vein patency, and its diameter was measured. Once the side had been chosen, the cannulation was performed following a sterile technique. All procedure were performed by Seldinger technique, with 22 Gauge IV catheter attached with 3 ml syringe as introducer needle. The vascular puncture was performed under ultrasound guidance, using a single-person technique. With transverse orientation, the transducer was placed transversally over the neck, and once the vein was visible in the middle of the ultrasound image, the needle was inserted in the plane perpendicular to the long axis of the transducer. With oblique orientation, the operator first obtained a transverse view of the vein and then rotated the transducer to 45 degrees (midway) between transverse and longitudinal view.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients age 3 months to 12 years old, weight 5-20 kg, male or female
  • who undergo heart surgery and indicated to have central venous cannulation
  • American Society of Anesthesiologist Physical Class 1-3
  • Family or representation of the patients agreed to participate in this study and sign informed consent

Exclusion criteria

  • history of surgery in the area of cannulation
  • already placed central venous cannulation <72 hours in the same venous
  • sign of infection, hematoma, emphysema, in the area of cannulation
  • history of cervical trauma
  • severe hemostatic disorder (International Normalized Ratio>2, thrombocyte <50.000, Prothrombin time>1.5 times, Activated Partial Thromboplastin Time > 1.5 times

Treatment and study plan

internal jugular venous cannulation

Procedure

internal jugular venous cannulation

Primary outcomes

  1. % of patients with successful cannulation in first attempt

    Time frame: at the procedure of cannulation

    The number of patients undergo cannulation with first attempt success are shown in percentage

Secondary outcomes

  1. % of patients with successful cannulation with designed approach

    Time frame: at the procedure of cannulation

    The number of patients undergo cannulation using designed approach are shown in percentage

Sponsors and collaborators

Lead sponsor

Indonesia University

Other

Registry information

Official study title

Oblique Versus Transverse Transducer Orientation Approach for Ultrasound Guided Internal Jugular Venous Cannulation in Heart Surgery Pediatric Patients

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Dec 19, 2022
Registry last updated
Dec 19, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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