Actively Recruiting

All Genders
NCT06604039

A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access Devices

Led by Teleflex · Updated on 2025-08-07

2500

Participants Needed

3

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The general objective of Teleflex's Vascular Access Device Registry (VADER) is to provide high-quality Level 3 (or better) data on the performance, safety and clinical benefits of Teleflex's vascular access devices when used in a real-world setting

CONDITIONS

Official Title

A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access Devices

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects will undergo a procedure that will include use of a Teleflex device covered by this Research.
  • Subject is willing and capable of providing informed consent and/or give approval to collect, store and process limited health information by the Sponsor; or such consent is provided by a legally designated representative if required by local law or regulation.
  • Subjects is able to read and understand English or Spanish languages
Not Eligible

You will not qualify if you...

  • Subject is currently participating in another clinical Registry or investigation that may confound the results of this Registry.
  • Subject was previously failed screening or was enrolled in this clinical Registry.
  • Subject is imprisoned
  • Subject is cognitively impaired and unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Huntsville Hospital

Huntsville, Alabama, United States, 35801

Actively Recruiting

2

Loma Linda University Health

Loma Linda, California, United States, 92354

Actively Recruiting

3

Tufts Medical Center

Boston, Massachusetts, United States, 02111

Actively Recruiting

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Research Team

A

Aderinola (Derin) Ogundimu, PhD, ACRP, PMP

CONTACT

T

Thomas E. Philbeck, Jr., PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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