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BD SiteRite(TM) 9 Ultrasound System - Clinical Study

NCT06632509 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 149

Last updated 2026-01-15

No results posted yet for this study

Summary

This post-market study is being conducted to generate safety and performance data on the SiteRite 9 System. The data will be utilized to support regional registrations (for example, EU MDR), and document any unforeseen residual risks.

Conditions

  • BD SiteRite 9 for VAD Insertion

Interventions

DEVICE

BD SiteRite(TM) 9

Ultrasound-guided vascular access device placement procedure using the BD SiteRite(TM) 9.

Sponsors & Collaborators

  • Becton, Dickinson and Company

    lead INDUSTRY

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-12
Primary Completion
2026-01-09
Completion
2026-01-09

Countries

  • United States

Study Locations

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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 NCT06632509 on ClinicalTrials.gov