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Success of Internal Jugular Vein Catheterization

Z

Zonguldak Bulent Ecevit University

Status

Completed

Conditions

Volume Status
Catheterization
Ultrasound

Treatments

Procedure: Internal Jugular Vein Catheterization

Study type

Interventional

Funder types

Other

Identifiers

NCT05717556
2018/12-6

Details and patient eligibility

About

Internal jugular vein cannulation can be performed with the blind technique under ultrasound (USG) guidance or using classical marker points. It has been shown that USG-guided interventions reduce the complication rate compared to the method performed with the blind technique (4%/13.5%). In addition, the initial entry success rate in the USG supported group is 65%. , this rate remained at 45% with the blind technique.

Although Pleth variability index monitoring is a noninvasive method, it is a technique that consistently predicts fluid sensitivity in patients under mechanical ventilation.

The aim of study is before applying USG guided catheterization; We think that by revealing the factors of the patient that are effective on the number of interventions, necessary measures can be taken for the success of catheterization as a result.

Enrollment

1 patient

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • aged 18-75
  • underwent coronary artery bypass surgery

Exclusion criteria

  • <18 years old
  • Hemodynamic instability
  • Use of inotropic agents

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1 participants in 2 patient groups

single attempt catheterization
Active Comparator group
Description:
successful catheterization with a single attempt number
Treatment:
Procedure: Internal Jugular Vein Catheterization
multiple attempts catheterization
Active Comparator group
Description:
successful catheterization after multiple attempts
Treatment:
Procedure: Internal Jugular Vein Catheterization

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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