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Clinical Trial Summary

The objective of this study is to determine the safety, performance, and effectiveness of the SeptRx IPO PFO Closure System in the treatment of Patent Foramen Ovale (PFO) in patients who are amenable to percutaneous closure of their PFO defects.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01385670
Study type Interventional
Source SeptRx, Inc.
Contact Beverly Tang, PhD
Phone 510-225-9170
Email beverly.tang@septrx.com
Status Recruiting
Phase N/A
Start date June 2011

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