Cardiovascular diseases
Conditions
Interventions
Group 1: • Cardiac magnetic resonance imaging (CMR) according to clinical indication
•In defined subgroups: magnetic resonance spectroscopy (MRS), including proton MRS (¹H-MRS) and/or phosphorus MRS (
Sponsors
Klinik für Kardiologie, Pneumologie und Angiologie am Universitätsklinikum Düsseldorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • ability to provide informed consent • Clinical indication for cardiac magnetic resonance imaging (CMR) • Ability to understand and comply with the instructions provided by the MRI staff
Exclusion criteria
Exclusion criteria: • Absence of written informed consent for study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the systematic collection and analysis of CMR-derived imaging parameters in patients with cardiovascular diseases and their association with clinical diagnoses and subsequent clinical outcomes | — |
Secondary
| Measure | Time frame |
|---|---|
| MRS-derived parameters (¹H-MRS and/or ³¹P-MRS), exercise CMR parameters obtained during MRI-compatible bicycle ergometry, and feasibility and image quality measures of the applied imaging techniques | — |
Countries
Germany
Contacts
Public ContactLisa Dannenberg
Clinical Trial Unit
Outcome results
None listed