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Completed

NCT Number: NCT02687126

Ultrasound Guided Technique for Internal Jugular Central Venous Catheterization in Pediatric Cardiac Surgical Patients

The purpose of the study is to evaluate the success rate using ultrasound as guidance during central venous cannulation in pediatric cardiac surgical patients.

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Key information

Age range

1 day–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Shahid Gangalal NationalHeart Centre

Kathmandu, Bagmati, 44606, Nepal

About this study

Central venous access may be essential in pediatric patients for fluid and a blood product administration, medication, parenteral nutrition, renal replacement therapy and hemodynamic monitoring. Obtaining central venous access in pediatric patients can be challenging, failure rates in pediatric patients range from 5% to 19% with reported complication rates from 2.5% to 22%. The landmark technique has been standard approach for many years. In comparison with landmark method, in pediatric patients, the use of ultrasound is associated with an increased success rate decreased operative time, reduced number of cannulation attempts , and a decreased number of carotid artery punctures. This study is designed to evaluate the success rate, complications, time taken for successful cannulation and their correlation with cross sectional area of the vein.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients requiring central venous catheterization for elective cardiac surgery.
  • Age below 15 years.

Exclusion criteria

  • Patient's guardian's refusal
  • Bleeding disorders
  • Clotting abnormalities (platelets count < 75,000/cumm, INR > 2)
  • Local site of infection
  • Underlying pneumothorax, pleural effusion or preoperative insertion of chest tube

Treatment and study plan

Central Venous Catheterization

Device

Ultrasound guided internal jugular venous catheterization

Primary outcomes

  1. Number of Attempts for Successful Central Venous Cannulation

    Time frame: up to 24 hours after intervention

    An attempt will be considered when complete withdrawal of the puncturing needle out of skin surface will occur

Secondary outcomes

  1. Time to Successful Cannulation

    Time frame: up to 1 hour after intervention

    Time from skin prick to blood aspiration via the catheter immediately following the guide-wire removal

  2. Number of Patients With Complications

    Time frame: up to 24 hours after intervention

    Arterial puncture, Hemothorax, Pneumothorax, Local site hematoma

Other outcomes

  1. Cross Sectional Area of Internal Jugular Vein

    Time frame: up to 1 hour before intervention

    Correlation of cross sectional area of internal jugular vein with number of attempts, time taken for successful cannulation and complication rate

Sponsors and collaborators

Lead sponsor

Shahid Gangalal National Heart Centre

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 22, 2016
Registry last updated
Apr 25, 2017

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.