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The SENTRY Clinical Study — SENTRY  

Pulmonary Embolism Clinical Trial

Official title:
A Prospective, Multi-Center Study of the Novate Sentry Bioconvertible Vena Cava Filter

Clinical Trial Summary

The SENTRY Bioconvertible Inferior Vena Cava (IVC) Filter has been developed to provide temporary protection against pulmonary embolism (PE).

Clinical Trial Description

Pulmonary embolism (PE) is a prevalent disease with a significant morbidity and mortality. The estimated annual incidence is 1.45 per 1,000 patients, which translates to 1,350,000 cases per year in the United States. It is estimated that PE results in more than 200,000 deaths per year. Currently there are two types of commercially available IVC filters utilized to prevent PE; permanent and retrievable. Both types of filters have documented limitations, such as tilting, migration, fracture, embolization and late deep vein thrombosis (DVT). Retrievable filters were developed to avert some of the late consequences of permanent filter, but in practice there is low success with eventual removal. In a series of 37 clinical studies, with a total of 6,834 patients the mean retrieval rate was 34%. There are numerous design features of the SENTRY IVC Filter that are intended to improve on the limitations of available IVC filters and obviate the need for retrieval. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01975090
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date September 2014
Completion date December 2018
View Details
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