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Recruiting NCT06845371

MELODY Registry Follow-Up Study

Observational Congenital Heart Disease (CHD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Congenital Heart Disease (CHD). Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Extension of the MELODY Registry, to assess longterm follow-up clinical results of Melody valve implantation after its commercialization in Europe / OUS

Primary outcome measures

  • primary outcome [Time frame: from december 2006 up to December 2027]
Secondary outcome measures (1)
  • secondary measure [Time frame: from december 2006 up to December 2027]

Eligibility criteria

Inclusion criteria

  • previous inclusion in the MELODY Registry

Exclusion criteria

  • none

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Germany · 1 center
  • University Hospital Tübingen — Tübingen

Identifiers

NCT: NCT06845371 · Melody

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗