What is the Purpose of this Study?
The purpose of this study is to further evaluate the performance of a device called the Celect Platinum Vena Cava Filter. The device is placed in the major vein (inferior vena cava) returning blood from the legs and pelvis to the heart to prevent blood clots from reaching the lungs (pulmonary embolism). The study will also evaluate the use of the Günther Tulip Retrieval Set for removing the filter. This type of study is known as a registry, in which data is collected on a number of people to see how they do in a real-world setting. Researchers intend to examine longer-term (up to 5 years) outcome data while the filter is in the inferior vena cava. The study will collect data about the patient’s Celect Platinum Vena Cava Filter procedure, the filter retrieval procedure, and any clinic visits or tests that are part of standard-of-care treatment.
Eligibility
- * A patient dataset is deemed suitable for inclusion if the patient has a procedure where a Celect Platinum Vena Cava Filter is placed
- * Subject has not previously participated in the Cook MDR-2126 study.
Where can I participate?
Beverly
More about this Clinical Trial
What is the full name of this clinical trial?
Post-market Celect Platinum Vena Cava Filters and Günther Tulip Retrieval Set Study