Ultrasound Guided Axillary Versus Jugular Central Venous Catheterization

Not Applicable

Completed

• Conditions: Critical Illness

• Registration Number: NCT02624323
• Lead Sponsor: Uniwersytecki Szpital Kliniczny w Opolu

Brief Summary

The main intention of this study is to compare two ultrasound-guided central venous catheterization procedures namely: real-time, ultrasound-guided, in plane axillary vein catheterization and real-time, ultrasound-guided, out of plane jugular vein catheterization in terms of venipuncture, catheterization success, early mechanical complication and catheter-related infection rate in mechanically ventilated patients admitted to the intensive care unit.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2015-11-29
• Study First Submitted QC: 2015-12-07
• Study First Posted: 2015-12-08
• Study Start: 2016-08
• Status Verified: 2020-08
• Primary Completion: 2020-08-03
• Study Completion: 2020-08-03
• Last Update Submitted: 2020-08-03
• Last Update Posted: 2020-08-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 614

Inclusion Criteria

• mechanically ventilated intensive care patients with clinical indications for central venous line placement

Exclusion Criteria

• trauma and hematoma at the catheterization site
• major blood coagulation disorders coincided with active bleeding
• anatomical abnormalities at the catheterization site
• infection at the catheterization site
• age less than 18 years
• lack of patients or closest relatives consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Procedure success rate	24 hours	to define catheterization success rate

Secondary Outcome Measures

Name	Time	Method
Incidence of catheter-related bloodstream infection	1 month	to assess the incidence of catheter-related bloodstream infection
Incidence of Catheter colonization	1 month	to assess the incidence of catheter colonization after removal
Procedure complication rate	24 hours	to assess the early mechanical complication rate

Trial Locations

Locations (2)

Department of Anesthesiology and Intensive Care, Uniwersytecki Szpital Kliniczny w Opolu; 🇵🇱 Opole, Silesia, Poland

2nd Department of Anesthesiology and Critical Care, Medical University of Lublin; 🇵🇱 Lublin, Poland