A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access Devices
Recruiting now
Conditions studied: Vascular Access Device
In brief
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
Key facts
- Study ID
- NCT06604039
- Run by
- Teleflex
- People needed
- 2500
- Starts
- 2024-12-08
- Expected to finish
- 2034-12-07
- Last updated by the study team
- 2025-08-07
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Huntsville Hospital — Huntsville, Alabama, United States (enrolling)
- Loma Linda University Health — Loma Linda, California, United States (enrolling)
- Tufts Medical Center — Boston, Massachusetts, United States (enrolling)
Full record on ClinicalTrials.gov
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