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Dual-plane Ultrasound Imaging During Vascular Access Procedures

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Mayo Clinic

Status

Completed

Conditions

Vascular Access Complication

Treatments

Device: Ultrasound probe
Device: Butterfly iQ+ ultrasound probe

Study type

Interventional

Funder types

Other

Identifiers

NCT05093699
21-007039

Details and patient eligibility

About

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

Enrollment

98 patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion 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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

98 participants in 2 patient groups

Control Group
Active Comparator group
Description:
Arterial line placement via standard mechanism; utilization of a single-plane ultrasound probe
Treatment:
Device: Ultrasound probe
Butterfly iQ+ ultrasound probe
Experimental group
Description:
Arterial line placement utilizing dual-plane, Butterfly iQ+ ultrasound probe
Treatment:
Device: Butterfly iQ+ ultrasound probe

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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