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Safety Study of Subclavian and Internal Jugular Venous Catheterization

Not Applicable
Conditions
Time to Insertion
Rates of Complications
Interventions
Device: Central venous catheter
Registration Number
NCT01196962
Lead Sponsor
E-DA Hospital
Brief Summary

There is no randomized controlled trial to compare the rates of complications associated with internal jugular and subclavian venous catheterization. The aim of this study is to compare mechanical, infectious, and thrombotic complications of internal jugular and subclavian venous catheterization. An improved understanding of CVC-related risks might help clinicians to choose one approach over the other in specific clinical settings.

Detailed Description

Central venous catheterization is often necessary to treat critically ill patients hospitalized in intensive care units (ICUs). However, this procedure may lead to serious and sometimes life-threatening complications, including mechanical, infectious, or thrombotic complications. The choice of insertion site can influence the incidence and type of such complications. The most frequently used sites for CVC insertion are the internal jugular and the subclavian vein. However, in an individual patient, criteria for choosing one approach over the other remain unclear.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
300
Inclusion Criteria
  • admission to ICU
  • requiring central venous catheterization
  • without contraindications to attempt both jugular and internal jugular access
Exclusion Criteria
  • the presence of a central venous catheter at admission
  • central venous catheterization within 2 weeks prior to admission
  • emergency catheterization for a life-threatening situation
  • major blood coagulation disorders
  • anatomic defect precluding catheterization at either site
  • skin lesions or recent surgery at either site

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Internal jugular veinCentral venous catheter-
Primary Outcome Measures
NameTimeMethod
Time to completely insertion1 hour
Secondary Outcome Measures
NameTimeMethod
rates of mechanical, infectious, and thrombotic complications14 days

Trial Locations

Locations (1)

E-Da hospital

🇨🇳

Kaohsiung, Taiwan

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