NCT00556426

Prospective, Multi-center, Single-arm Study to Assess the Safety of Retrieval of the Recovery G2 Filter.

The Bard® Recovery® Filter Registry (EVEREST) for Patients Who Are Candidates for an Optional (Retrievable) Inferior Vena Cava Filter That Undergo Placement of the Bard® Recovery® Filter.

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 100 (actual)
• Sponsor: C. R. Bard · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study was designed to assess the safety of retrieval of the Bard Recovery® G2® Filter System. The G2 filter is an FDA-cleared device for inferior vena caval interruption in patients with pulmonary thromboembolism.

Conditions

• Pulmonary Embolism
• Venous Thromboembolic Disease

Interventions

Type	Name	Description
DEVICE	Bard Recovery G2 Filter System	Retrieval of previously placed RECOVERY G2 IVC filter

Timeline

• Start date: 2005-12-01
• Primary completion: 2007-04-01
• Completion: 2007-04-01
• First posted: 2007-11-12
• Last updated: 2012-06-01
• Results posted: 2011-05-11