Axillary Vein Cannulation: 'Hockey' Probe Versus Linear Probe
Comparing Axillary Vein Cannulation with 'Hockey' Probe Versus Linear Probe for Central Venous Access
1 other identifier
observational
100
1 country
1
Brief Summary
Central venous catheterization, specifically through the axillary vein, is a procedure of critical importance in various clinical contexts. Site selection is dependent on clinical assessment, experience and the physician preference. This study aims to evaluate the potential advantages of using the "hockey stick" ultrasonography probe for axillary vein cannulation and determine whether this probe enhances axillary vein imaging, accelerates the central vein cannulation procedure and reduces the rate of complications compared to the linear probe. Methods: 100 participants were recruited and allocated into two groups: the linear probe group and the hockey stick probe group. All procedures were performed by two senior anesthesia and intensive care residents, each with experience of over 100 central vascular access procedures. Follow-up chest X-rays were taken two hours post-procedure to verify the correct position of the catheter and to rule out complications such as pneumothorax, hemothorax, cardiac tamponade, and incorrect line placement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2022
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2024
CompletedFirst Submitted
Initial submission to the registry
December 30, 2024
CompletedFirst Posted
Study publicly available on registry
February 3, 2025
CompletedFebruary 3, 2025
December 1, 2024
2.2 years
December 30, 2024
January 29, 2025
Conditions
Outcome Measures
Primary Outcomes (4)
Success on first attempt
An attempt is defined by every needle direction change. Whenever vein puncture was not achieved by a simple, straight movement without any change of direction in any plane this cannulation was not counted as success at first attempt
24 hours
Number attempts
An attempt is defined by every needle direction change. Whenever vein puncture was not achieved by a simple, straight movement without any change of direction in any plane this cannulation was not counted as success at first attempt
24 hours
Procedure Time
The procedure time measurement stops when skin dressing is applied. Time measurement was done by an independent observer.
24 hours
Cumulative number of complications
Complications early and late were recorded either with ultrasonography immedi-ately after the procedure or in the chest X-ray 2 hours after.
24 hours
Study Arms (2)
Hockey ultrasound probe
Use of Hockey ultrasound probe for axillary vein cannulation
Linear ultrasound probe
Use of linear ultrasound probe for axillary vein cannulation
Interventions
This study aims to evaluate the potential advantages of using the "hockey stick" ultrasonography probe for axillary vein cannulation and determine whether this probe enhances axillary vein imaging, accelerates the central vein cannulation procedure and reduces the rate of complications compared to the linear probe
Eligibility Criteria
Patient scheduled for elective placement of the central venous catheter in the axillary vein.
You may qualify if:
- age above 18 years old
- scheduled for elective central venous catheter in the axillary vein
You may not qualify if:
- medical contraindication for axillary vein cannulation (coagulation abnormalities, local skin infection or chest wall deformation)
- patient consent decline
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
II Klinika Anestezjologii i Intensywnej Terapii
Warsaw, Poland
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 30, 2024
First Posted
February 3, 2025
Study Start
May 1, 2022
Primary Completion
July 1, 2024
Study Completion
July 1, 2024
Last Updated
February 3, 2025
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share