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UnknownNCT02220270

Hyperion™ International Registry Trial

A Prospective, Multi-center Study to Evaluate the Safety and Performance of the Hyperion™ ASD and PDA Closure Systems.

Status
Unknown
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
European Cardiovascular Research Center · Network
Sex
All
Age
1 Year – 90 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the safety, performance and efficacy of the Hyperion™ Occluder Systems during treatment of ASD and PDA patients.

Conditions

Interventions

TypeNameDescription
DEVICEASD and PDA closure

Timeline

Start date
2015-05-01
Primary completion
2016-11-01
Completion
2017-08-01
First posted
2014-08-19
Last updated
2015-08-19

Locations

10 sites across 4 countries: Algeria, China, France, Germany

Source: ClinicalTrials.gov record NCT02220270. Inclusion in this directory is not an endorsement.

Hyperion™ International Registry Trial (NCT02220270) · Clinical Trials Directory