Ultrasound-guided Axillary Artery vs Femoral Artery Cannulation.

Not Applicable

Completed

• Conditions: Critical Illness

• Registration Number: NCT02801825
• Lead Sponsor: Uniwersytecki Szpital Kliniczny w Opolu

Brief Summary

The main purpose of the study is to compare two ultrasound-guided arterial cannulation procedures: in-plane infraclavicular axillary artery cannulation and out-of-plane femoral artery cannulation.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-06-07
• Study First Submitted QC: 2016-06-12
• Study First Posted: 2016-06-16
• Study Start: 2018-01-22
• Primary Completion: 2020-10-01
• Study Completion: 2021-08-01
• Status Verified: 2021-12
• Last Update Submitted: 2021-12-19
• Last Update Posted: 2021-12-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 110

Inclusion Criteria

mechanically ventilated critically ill patients with indications for artery cannulation:

• in whom radial artery cannulation is unable to perform or
• in order to conduct hemodynamic monitoring using transpulmonary thermodilution

Exclusion Criteria

• age less than 18 years
• trauma and hematoma at the catheterization site
• clinically significant coagulation disorders
• infection at the catheterization site
• lack of patients or closest relatives contents
• precedent surgery operation into the femoral and axillary arteries
• clinically significant ischemia of the limb at the cannulation side

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Cannulation success rate	24 hours	The goal of the assessment of the cannulation success rate is essential for the estimation of the usefulness of both artery approaches in clinical practice.

Secondary Outcome Measures

Name	Time	Method
Number of puncture attempts.	24 hours	The goal of the assessment is the evaluation which approach is easier to perform.
Procedure complication rate.	24 hours	The goal of the assessment of the early mechanical complication rate is crucial for the estimation of the safety of both procedures in clinical practice.

Trial Locations

Locations (1)

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