BD Prevue(TM) II Peripheral Vascular Access System With Cue(TM) Needle Tracking Technology Clinical Study
Completed
Conditions studied: BD Prevue II for Peripheral Intravenous Catheter Placement
In brief
This post-market study is being conducted to generate safety and performance data on the BD Prevue(TM) II Peripheral Vascular Access System with Cue(TM) Needle Tracking Technology. The data will be utilized to support regional registrations (for example, EU MDR), and document any unforeseen residual risks.
Key facts
- Study ID
- NCT06632496
- Run by
- Becton, Dickinson and Company
- People needed
- 156
- Starts
- 2025-03-28
- Expected to finish
- 2025-09-23
- Last updated by the study team
- 2026-01-16
Who can join
Age: 1 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 1 years, or older
- A patient who is a candidate for an ultrasound-guided peripheral intravenous catheter (midline catheters included) placement procedure using BD PrevueTM II Peripheral Vascular Access System with CueTM Needle Tracking Technology as assessed per their clinician(s)
- Able and willing to provide informed consent or legal authorized representative (LAR) authorized to give consent on behalf of the subject
You may not qualify if…
- Any patient in whom ultrasound procedure might interfere with medical care or create undue hardship
- Known, or suspected, allergy to materials contained in the BD PrevueTM II Peripheral Vascular Access System with CueTM Needle Tracking Technology or accessories that may come in contact with the patient
- Localized skin, tissue, or other clinical factors that would prevent completion of the ultrasound procedure
- Previous medical history that would prevent completion of the ultrasound procedure
Where it is running
- Brookdale University Hospital & Medical Center — Brooklyn, New York, United States
- Allegheny Health Network Research Institute — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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