Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation: ZEROFLUOROAXI TRIAL (ZEROFLUOROAXI)
Primary Purpose
Arrhythmias, Cardiac, Venous Puncture, Implantable Defibrillator User
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Ultrasound Guided Axillary Venous Access
Fluoroscopy-Guided Axillary Venous Access
Sponsored by
About this trial
This is an interventional treatment trial for Arrhythmias, Cardiac focused on measuring pacemaker, ICD, arrhythmias, Cardiac Implantable Electronic Device, Vascular access, Venous puncture, Ultrasound, Fluoroscopy
Eligibility Criteria
Inclusion Criteria:
- Need of a standard transvenous pacemaker or implantable cardioverter defibrillator implantations
- Age > 18 years
Exclusion Criteria:
- Leadless pacemaker or subcutaneous ICD
Sites / Locations
- Azienda Ospedaliero-Universitaria di Ferrara
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Ultrasound Guided Axillary Access
Fluoroscopic Guided Axillary Access
Arm Description
Direct visualization of axillary vein with ultrasound will be obtained and used as a guidance for venous puncture.
Standard technique: using the intersection of the lateral borders of the second and third rib as a radiological landmarks.
Outcomes
Primary Outcome Measures
Composite of pneumothorax, pocket hematoma, arterial puncture, pocket or device infection, hemothorax at 30 days.
Composite of pneumothorax, pocket hematoma, arterial puncture, pocket or device infection, hemothorax at 30 days.
Secondary Outcome Measures
Full Information
NCT ID
NCT05101720
First Posted
October 20, 2021
Last Updated
February 5, 2023
Sponsor
University Hospital of Ferrara
1. Study Identification
Unique Protocol Identification Number
NCT05101720
Brief Title
Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation: ZEROFLUOROAXI TRIAL
Acronym
ZEROFLUOROAXI
Official Title
Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
November 30, 2022 (Actual)
Study Completion Date
December 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital of Ferrara
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Single center, randomized trial (1:1 fashion) to asses the safety and the feasibility of the ultrasound guided venous puncture vs standard fluoroscopic technique in patients undergoing pacemaker or implantable cardioverter-defibrillator implantations.
Detailed Description
Rationale: axillary, cephalic and subclavian venous accesses are commonly used in pacemaker and implantable cardioverter defibrillator implantations. Axillary puncture and cephalic vein surgical cutdown are both recommended in international guidelines due to low risk of pneumothorax and chronic lead complications. Sometimes cephalic vein is not available. Today axillary puncture is performed under fluoroscopic view and some complications still exist with this venous access as pneumothorax and arterial puncture. Axillary vein direct visualization can be obtained with standard venography or with ultrasound. With direct visualization and puncture of the axillary vein under ultrasound guidance venography with radiocontrast could be avoided. Less radiation exposure for patient and operator and direct visualization of the needle are possible with lower periprocedural complications using ultrasound. Despite the great interest for ultrasound guided axillary puncture up today we have few data on its feasibility. Our hypothesis is that ultrasound guided axillary access is more safe and more feasible than the standard fluoroscopic technique.
We decided to enroll all the patients undergoing standard transvenous pacemaker or cardioverter implantable defibrillator. We randomize the patients with 1:1 fashion to axillary venous access under fluoroscopic guidance or to ultrasound guided axillary venous access.
Obiectives: to asses safety, feasibility of the ultrasound guided venous puncture.
Main Endpoint: composite of pneumothorax, pocket hematoma, arterial puncture, pocket or device infection, hemothorax at 30 days.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arrhythmias, Cardiac, Venous Puncture, Implantable Defibrillator User, Pacemaker Complication, Vascular Access Complication, Fluoroscopy; Adverse Effect
Keywords
pacemaker, ICD, arrhythmias, Cardiac Implantable Electronic Device, Vascular access, Venous puncture, Ultrasound, Fluoroscopy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
280 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ultrasound Guided Axillary Access
Arm Type
Experimental
Arm Description
Direct visualization of axillary vein with ultrasound will be obtained and used as a guidance for venous puncture.
Arm Title
Fluoroscopic Guided Axillary Access
Arm Type
Active Comparator
Arm Description
Standard technique: using the intersection of the lateral borders of the second and third rib as a radiological landmarks.
Intervention Type
Procedure
Intervention Name(s)
Ultrasound Guided Axillary Venous Access
Intervention Description
Direct visualization of axillary vein will be obtained with ultrasound sterile linear probe.
Intervention Type
Procedure
Intervention Name(s)
Fluoroscopy-Guided Axillary Venous Access
Intervention Description
Fluoroscopic landmarks will be used and axillary venous puncture will be performed without ultrasound
Primary Outcome Measure Information:
Title
Composite of pneumothorax, pocket hematoma, arterial puncture, pocket or device infection, hemothorax at 30 days.
Description
Composite of pneumothorax, pocket hematoma, arterial puncture, pocket or device infection, hemothorax at 30 days.
Time Frame
One month after index procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Need of a standard transvenous pacemaker or implantable cardioverter defibrillator implantations
Age > 18 years
Exclusion Criteria:
Leadless pacemaker or subcutaneous ICD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matteo Bertini, MD, PhD
Organizational Affiliation
Università degli Studi di Ferrara
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliero-Universitaria di Ferrara
City
Ferrara
ZIP/Postal Code
44124
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation: ZEROFLUOROAXI TRIAL
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