Registry for adults with congenital heart disease (ACHD) with abnormal ventricular function and/or heart failure
Recruiting
- Conditions
- Q20Q21Q24Q22Q23Q25Q26Q27Q28Congenital malformations of cardiac chambers and connections
- Registration Number
- DRKS00030508
- Lead Sponsor
- Deutsches Herzzentrum München
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1500
Inclusion Criteria
Minimum age 18 years, patient at one of the participating centers, consent to participate in the study
Exclusion Criteria
Failure to meet inclusion criteria
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method (1) Establishment of a registry on heart failure in ACHD (real world data)<br><br>(2) Definition of predictors for morbidity and mortality <br><br>(3) Implementation of measures for long-term improvement of the biopsychosocial situation of ACHD with heart failure or/and abnormal ventricular function<br><br>(4) Development of hypotheses for prospective multicenter therapy studies<br>
- Secondary Outcome Measures
Name Time Method - Improve the care of ACHD with heart failure by expanding the previously limited data base, based on older studies that include only small numbers of patients and short observation periods <br>- Increased knowledge through review and improved, more comprehensive documentation of current standards of care. <br>- Generation of evidence-based data on long-term prognosis, treatment regimens, patient safety, quality of care, etc.<br>- Development of measures to improve care (e.g., early detection, targeted interventions, ...)<br>- Development of specific measures for prevention and health promotion in ACHD with heart failure