DRKS00010273RecruitingNot Applicable
ong Term Surveillance of Patients with Right ventricular outflow tract dysfunction treated by surgical conduit implantation versus percutaneous pulmonary valve implantation with Melody Valve
Deutsches Herzzentrum München0 sites400 target enrollmentStarted: April 14, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 400
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 5 Years to 90 Years (—)
- Sex
- All
Inclusion Criteria
- •All patients >= 5 years who received either a percutaneous Melody valve
- •or a biological conduit for RVOT dysfunction at the German Heart Centre Munich since 2006
- •-Patient informed consent / data release form
Exclusion Criteria
- •Patients < 5 years of age
- •Previous percutaneous valve implantation
- •No Patient informed consent
Investigators
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