I25
Conditions
Interventions
Group 1: The goal is the optimization of magnetic resonance imaging for cardiovascular and pulmonary imaging. After implementation of new sequences / measurement methods, these will be tested in volun
Sponsors
Universitätsklinikum Ulm, Kliniken am oberen Eselsberg
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: healthy volunteers patients with cardiovascular disease patients with pulmonary disease
Exclusion criteria
Exclusion criteria: • Non-consenting patients / subjects • The presence of pregnancy or unsafe contraception • Patients / subjects with cardiac instability (acute myocardial infarction < 7 days, decompensated heart failure) • Patients / subjects with pronounced claustrophobia Patients / subjects with pacemakers or implanted defibrillators (ICD) • Patients / subjects with metal splinter injury to the eyes or MRI-incompatible metallic inclusions or implants • Patients / subjects with larger tattoos • Patients / subjects with non-removable piercings • Patients / subjects participating in another study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of the study is the evaluation of new MR sequences for thoracic and cardiovascular imaging. In this context, new measurement techniques (in particular methods for the quantification of myocardial function and tissue properties, the assessment of the lung parenchyma and lung function) will be implemented and initially evaluated in volunteers and patients. Contrast agents will not be administered. | — |
Countries
Germany
Contacts
Public ContactDominik Buckert
Ulm Unievrsity Medical CenterCenter of Internal Medicine
Outcome results
None listed