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

Recruitingn/aAges any - anyAllTeleflex
NCT06604039 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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

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📋 Eligibility rules (as published)
Inclusion Criteria: * 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 Exclusion Criteria: * 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
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What it tests

  • Central venous catheter
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Where

3 sites
Huntsville Hospital
Huntsville, United States
Loma Linda University Health
Loma Linda, United States
Tufts Medical Center
Boston, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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