POCUS for Difficult Peripheral Access in the Emergency Department - a RCT
Primary Purpose
Vascular Access, Emergencies
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
bi-plane sonographic view to difficult peripheral vascular access using Butterfly iQ+®
Sponsored by

About this trial
This is an interventional other trial for Vascular Access focused on measuring Point-of-care ultrasound, emergency department
Eligibility Criteria
Inclusion Criteria: at least one of the following criteria have to be present along with the need for a peripheral access
- chronic renal disease/ongoing dialysis;
- sickle cell anemia;
- prolonged and/or frequent use of i.v. drugs;
- difficult vascular access (after a first attempt or self-reported);
- previously need for more than one attempts / ultrasound guidance for getting a peripheral vascular access.
Exclusion Criteria:
- no consent to participate in the study.
Sites / Locations
- Emergency Department, Città della Salute e della Scienza di Torino Univeristy Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
mono-plane sonographic view
bi-plane sonographic view
Arm Description
Usual standard of care, in our institution, for difficult peripheral vascular access in the Emergency Department.
Outcomes
Primary Outcome Measures
number of attempts of each peripheral i.v. access placement
The number of attempts needed for getting a peripheral i.v. access will be measured
Time needed for each peripheral i.v. access placement
Time needed for for getting a peripheral i.v. access will be measured
Secondary Outcome Measures
Full Information
NCT ID
NCT05119673
First Posted
October 20, 2021
Last Updated
May 8, 2023
Sponsor
University of Turin, Italy
Collaborators
Butterfly Network
1. Study Identification
Unique Protocol Identification Number
NCT05119673
Brief Title
POCUS for Difficult Peripheral Access in the Emergency Department - a RCT
Official Title
Point-of-care Ultrasound for Difficult Peripheral Vascular Access in the Emergency Department - a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
October 22, 2021 (Actual)
Primary Completion Date
May 11, 2022 (Actual)
Study Completion Date
May 11, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Turin, Italy
Collaborators
Butterfly Network
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Peripheral intravenous line insertion is the most commonly performed invasive procedure in the emergency department (ED). The research hypothesis is that a biplane sonographic approach (i.e., an out-of-plane and in-plane view) might be superior to a mono-plane approach (i.e., an out-of-plane or in-plane view) obtaining a peripheral vascular access among difficult patients admitted to the ED
Detailed Description
Peripheral intravenous line insertion is the most commonly performed invasive procedure in the emergency department (ED). In some studies, difficult vascular access population was about 33% of evaluated patients and for most of them the "blind" method (i.e., palpation) fails in the line insertion. Ultrasound guidance often increase the success rate among these patients.
Two basic techniques were proposed for sonographic guidance, a transversal or a longitudinal approach to the chosen vessel (i.e., out-of-plane or in-plane view, respectively, "mono-plane" approach).
The availability of hand-held sonographic devices is increasing the number of emergency department were this guidance is used in a difficult vascular access population.
The Butterly iQ+ device is now able to show out-of-plane and in-plane views, simultaneously, the so called bi-plane view.
Aim of this randomized controlled trial is to test if a bi-plane sonographic vision might be able to increase the performance of trained operators in obtaining a peripheral vascular access among difficult patients admitted to the ED.
The present study will be a randomized controlled, 2-arm, nonblinded trial held at the Città della Salute e della Scienza di Torino, University hospital, Turin, Italy.
All healthcare workers already trained in ultrasound-guided vascular access will be considered eligible for the study (i.e., emergency physicians, residents, nurses) after an ad hoc brief (2 hours) training on the study.
This will be a "real world" study, each provider will be free of choosing the device he/she thought appropriate for each patient (in terms of length, gauge, type - peripheral midline will be included in the Italian center).
Using a computerized permuted blocks of random sizes, enrolled patients will be randomized in a 1:1 ratio to be evaluated using either the "standard" ultrasound-guided approach (out-of-place or in-plane view) or the bi-plane view (i.e. out-of-place and in-plane view, simultaneously).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Access, Emergencies
Keywords
Point-of-care ultrasound, emergency department
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
442 (Actual)
8. Arms, Groups, and Interventions
Arm Title
mono-plane sonographic view
Arm Type
No Intervention
Arm Description
Usual standard of care, in our institution, for difficult peripheral vascular access in the Emergency Department.
Arm Title
bi-plane sonographic view
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
bi-plane sonographic view to difficult peripheral vascular access using Butterfly iQ+®
Intervention Description
Bi-plane Butterfly iQ+® sonographic visualization will be used to help Emergency Department operators to get a venous peripheral access in a population of patients considered difficult for this task based on their history or the present clinical situation.
Primary Outcome Measure Information:
Title
number of attempts of each peripheral i.v. access placement
Description
The number of attempts needed for getting a peripheral i.v. access will be measured
Time Frame
Through study completion, likely of 1 year and half
Title
Time needed for each peripheral i.v. access placement
Description
Time needed for for getting a peripheral i.v. access will be measured
Time Frame
Through study completion, likely of 1 year and half
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: at least one of the following criteria have to be present along with the need for a peripheral access
chronic renal disease/ongoing dialysis;
sickle cell anemia;
prolonged and/or frequent use of i.v. drugs;
difficult vascular access (after a first attempt or self-reported);
previously need for more than one attempts / ultrasound guidance for getting a peripheral vascular access.
Exclusion Criteria:
no consent to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emanuele Pivetta, MD,PhD
Organizational Affiliation
Città della Salute e della Scienza di Torino University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emergency Department, Città della Salute e della Scienza di Torino Univeristy Hospital
City
Turin
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
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POCUS for Difficult Peripheral Access in the Emergency Department - a RCT
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