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Study identifier: NCT06604039 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Vascular Access Device  ·  Sponsor: Teleflex

PhaseN/A
Planned participants2500
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Aderinola (Derin) Ogundimu, PhD, ACRP, PMP  ·  469.569.9223  ·  aderinola.ogundimu@teleflex.com

Thomas E. Philbeck, Jr., PhD  ·  2107227438  ·  thomas.philbeck@teleflex.com

Always discuss trial participation with your own doctor first.

Locations (3)

Huntsville HospitalHuntsville, Alabama, United StatesRecruiting
Loma Linda University HealthLoma Linda, California, United StatesRecruiting
Tufts Medical CenterBoston, Massachusetts, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06604039