Registry for patients with valvular heart disease undergoing interventions
Valvular Heart Disease Registry - Observational Study of Percutaneous Valvular Interventions
This study collects information from patients with serious heart valve problems who are getting a specific heart procedure to see how well it works and how they do over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Technical University of Munich Academic / other |
| Locations | 1 site (München) |
| Trial ID | NCT03488732 on ClinicalTrials.gov |
What this trial studies
This registry collects and analyzes data from patients with severe valvular defects who are undergoing transcatheter valvular interventions. It aims to gather baseline, procedural, and follow-up information to address various issues related to these percutaneous procedures. The observational nature of the study allows for a comprehensive understanding of patient outcomes and treatment efficacy over time.
Who should consider this trial
Good fit: Ideal candidates for this registry are patients with severe valvular defects who are scheduled for a transcatheter valvular intervention.
Not a fit: Patients who are unable to provide informed consent will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could improve the management and outcomes of patients with valvular heart disease by providing valuable insights into treatment effectiveness.
How similar studies have performed: Other registries focusing on transcatheter interventions have shown success in improving patient outcomes and understanding treatment impacts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Severe valvular defect planned for valvular intervention Exclusion Criteria: \- No informed consent
Where this trial is running
München
- Klinik für Innere Medizin I — München, Germany (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.