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Clinical Trial Summary

prospective randomized double-blind controlled study


Clinical Trial Description

Total of 69 ASA (American Society of Anesthesiologist) physical status class I or II patients will be enrolled.

Randomly assigned to three group according to the depth of guide-wire prior to tissue dilation during central catheterization via right internal jugular vein. (Group 1: 15 cm / Group 2: 17.5 cm / Group 3: 20 cm)

Central catheterization will be performed by anesthesiologists who be blinded to this study protocol.

An investigator will monitor and record whether any arrhythmia will occur.

The incidence of occurrence of arrhythmia will be compared between three groups. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Patient Safety During Central Venous Catheterization

NCT number NCT02711761
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date May 2016

See also
  Status Clinical Trial Phase
Completed NCT03116724 - Direct Measurement of Ideal Depth of Central Line N/A