N/A
N=98
Dual-plane Ultrasound Imaging During Vascular Access Procedures
Vascular Access Complication
Bottom Line
View on ClinicalTrials.gov: NCT05093699 ↗Enrolled (actual)
98
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Time to Successful First Stick in Minutes — 4.56; 6.24 minutes
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Butterfly iQ+ ultrasound probe (Device); Ultrasound probe (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Mayo Clinic
- Primary completion
- Jun 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Successful First Stick in Minutes |
4.56; 6.24 | — |
| SECONDARY Number of Attempts for Successful Cannulation |
48; 39 | — |
| SECONDARY Amount of Time Required for Successful Arterial Catheter Cannulation |
4.56; 6.24 | — |
| SECONDARY Number of Failed Attempts for Cannulation |
2; 9 | — |
Summary
Researchers are evaluating the clinical efficiency of utilization of a dual-plane simultaneous view ultrasound probe (Butterfly iQ+; Butterfly Network, Inc.) during arterial catheter placement in the operating room
Eligibility Criteria
Inclusion criteria
- Patient: Elective surgical patients requiring non-emergent ultrasound-guided radial arterial catheter placement
- Providers: Anesthesia providers to include trainees, certified registered nurse anesthetists (CRNA) and attending anesthesia providers.
Exclusion Criteria
- Patient
- Pregnant
- Patients in a moribund state or palliative care only
- Vulnerable patients (i.e. Severe mental handicap, non-decisional)
- History of peripheral arterial disease
- Placement of arterial catheter without ultrasound guidance
- Provider: Medical students or CRNA students.
Data sourced from ClinicalTrials.gov (NCT05093699). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.