Hyperion™ International Registry Trial
NCT02220270 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2015-08-19
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
- Atrial Septal Defects
- Patent Ductus Arteriosus
Interventions
- DEVICE
-
ASD and PDA closure
Sponsors & Collaborators
-
Comed B.V.
collaborator INDUSTRY -
European Cardiovascular Research Center
lead NETWORK
Eligibility
- Min Age
- 1 Year
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-05-31
- Primary Completion
- 2016-11-30
- Completion
- 2017-08-31
Countries
- Algeria
- China
- France
- Germany
Study Locations
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