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UnknownNCT01385670

InterSEPT: In-Tunnel SeptRx European PFO Trial

InterSEPT: In-Tunnel SeptRx European PFO Trial: A Prospective, Multi-Center Study to Evaluate the Safety and Performance of the SeptRx IPO PFO Closure System

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
SeptRx, Inc. · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICETranscatheter PFO closure with the SeptRx Intrapocket PFO Occluder (IPO)Transcatheter PFO closure

Timeline

Start date
2011-06-01
Primary completion
2012-06-01
First posted
2011-06-30
Last updated
2011-06-30

Locations

2 sites across 2 countries: France, Germany

Source: ClinicalTrials.gov record NCT01385670. Inclusion in this directory is not an endorsement.

InterSEPT: In-Tunnel SeptRx European PFO Trial (NCT01385670) · Clinical Trials Directory