MedTrace Logo

BD Prevue(TM) II Peripheral Vascular Access System With Cue(TM) Needle Tracking Technology Clinical Study

NCT06632496 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 156

Last updated 2026-01-16

No results posted yet for this study

Summary

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.

Conditions

  • BD Prevue II for Peripheral Intravenous Catheter Placement

Interventions

DEVICE

BD Prevue(TM) II

Ultrasound-guided peripheral intravenous catheter placement procedure using the BD Prevue(TM) II

Sponsors & Collaborators

  • Becton, Dickinson and Company

    lead INDUSTRY

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-28
Primary Completion
2025-09-23
Completion
2025-09-23

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06632496 on ClinicalTrials.gov