Interventional Structural Registry - LuEbeck
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: Structural Heart Disease. Basic parameters: from 18 years · 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 →
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Overview
The aim of the registry is to investigate the effect of catheter-assisted procedures in the context of structural heart disease on clinical morbidity and mortality. Furthermore, the long-term prognosis of patients after a catheter-based procedure is to be evaluated. In particular, the following parameters will be documented and the following questions discussed: * Underlying and concomitant diseases of these patients * Evaluation of the methods in relation to the respective disease * Safety - acute and long-term * Effectiveness - periprocedural, hospital and long-term course * Concomitant therapies
Primary outcome measures
- Combined endpoint [Time frame: 30days]
Eligibility criteria
Inclusion criteria
- Structural heart disease
Exclusion criteria
- Patients without consent/information
- Age ≤ 18 years
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
- Other
Study locations
Germany · 1 center
- Universitätsklinikum Schleswig-Holstein — Lübeck
Identifiers
NCT: NCT06977139 · 21-330 · 21-330