Utility of Ultrasonography During Internal Jugular Vein Catheterisation in Pediatric Patients

Complication Rate Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02131519
• Other study ID #: 13968
• Secondary ID: USG13968
• Status: Completed
• Phase: N/A
• First received: May 4, 2014
• Last updated: May 5, 2014
• Start date: January 2012
• Est. completion date: March 2014

Study information

• Verified date: May 2014
• Source: Ankara University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Turkey: Ministry of Health
• Study type: Observational

Clinical Trial Summary

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. We wanted to evaluate our success rate using ultrasound as a guidance during central vein insertion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 180
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 1 Month to 16 Years

Eligibility

Inclusion Criteria:

• pediatric patients required internal jugular vein catheter

Exclusion Criteria:

• aged smaller than 1 month

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Complication Rate
• Number of Trials

Intervention

Procedure:
• internal jugular vein catheter placement

Locations

Country	Name	City	State
Turkey	Ankara University	Ankara
Turkey	Ankara University, Pediatric Surgery	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Ankara University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	effect of experience		during anesthesia	No
Primary	success rate		during anesthesia	No
Secondary	complication rate		during anesthesia	No